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A Randomized Trial to Evaluate Sequential vs Simultaneous Patching (ATS22)

Primary Purpose

Amblyopia

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Patching
Glasses
Sponsored by
Jaeb Center for Health Research
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Amblyopia focused on measuring patching, glasses, spectacles, simultaneous, sequential

Eligibility Criteria

3 Years - 13 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Age 3 to <13 years at the time of randomization
  2. Amblyopia associated with anisometropia, strabismus, or both

    o Criteria for strabismic amblyopia: At least one of the following must be met:

    • Presence of a heterotropia on examination at distance or near fixation (with or without optical correction)
    • Documented history of strabismus which is no longer present (which in the judgment of the investigator could have caused amblyopia)

      • Criteria for anisometropia: At least one of the following criteria must be met:

        • 1.00 D difference between eyes in spherical equivalent (SE)
        • 1.50 D difference in astigmatism between corresponding meridians in the two eyes
      • Criteria for combined-mechanism amblyopia: Both of the following criteria must be met:
    • Criteria for strabismus are met (see above)

      • 1.00 D difference between eyes in spherical equivalent OR ≥1.50 D difference in astigmatism between corresponding meridians in the two eyes
  3. No previous treatment for amblyopia, including no more than 24 hours of spectacle wear.
  4. Investigator planning to initiate spectacle correction of refractive error meeting the following criteria based on a cycloplegic refraction that has been performed within 30 days:

    1. Full correction of anisometropia
    2. Full correction of astigmatism with the same axis found by the cycloplegic refraction
    3. Full correction of any myopia
    4. Hyperopia must not be under corrected by more than 1.50 D, and reduction in plus sphere must be symmetric in the two eyes.
  5. At enrollment, single VA measured in each eye assessed in trial frames with the spectacle correction the investigator plans to prescribe, using the investigator's routine method as follows:

    • VA in the amblyopic eye 20/40 to 20/200 inclusive.
    • Age-normal VA in the fellow eye:40,41

      • 3 years: 0.4 logMAR (20/50) or better
      • 4 years: 0.3 logMAR (20/40) or better
      • 5-6 years: 0.2 logMAR (20/32) or better
      • 7-12 years: 0.12 logMAR (78 letters) or better
    • Interocular difference ≥ 3 logMAR lines (0.3 logMAR) or ≥ 15 letters o When participants return for the Spectacle Baseline / Randomization Visit with their new spectacles, they will need to meet the same criteria as above using the ATS-HOTV or E-ETDRS protocol after wearing the new spectacles for at least 10 minutes (based upon the mean of a test and retest of VA in those new spectacles).
  6. Investigator is willing to prescribe spectacle wear followed sequentially by patching or simultaneous spectacles and patching treatment per protocol.
  7. Parent understands the protocol and is willing to accept randomization.
  8. Parent has phone (or access to phone) and is willing to be contacted by Jaeb Center staff or other study staff.
  9. Relocation outside of area of an active PEDIG site for this study within the next 56 weeks is not anticipated.

Exclusion Criteria:

  1. Myopia greater than -6.00 D spherical equivalent in either eye.
  2. Previous intraocular or refractive surgery.
  3. Planned strabismus surgery in the next 56 weeks.
  4. Any previous treatment for amblyopia (patching, atropine, Bangerter filter, vision therapy, or binocular treatment).
  5. Previous spectacle or contact lens wear for more than 24 hours.
  6. Parent and participant willing to forego option of contact lens wear for the duration of the study.
  7. Ocular co-morbidity that may reduce VA determined by an ocular examination performed within the past 7 months (Note: nystagmus per se does not exclude the participant if the above VA criteria are met).
  8. Severe developmental delay that would interfere with treatment or evaluation (in the opinion of the investigator). Participants with mild speech delay or reading and/or learning disabilities or attention deficit hyperactivity disorder (ADHD) are not excluded.
  9. Known allergy to adhesive patches.
  10. Known allergy to silicone.

Sites / Locations

  • University of Alabama at BirminghamRecruiting
  • Midwestern University Eye InstituteRecruiting
  • University of ArizonaRecruiting
  • Marshall B. Ketchum UniversityRecruiting
  • Loma Linda University Health Care, Dept. of OphthalmologyRecruiting
  • Stanford UniversityRecruiting
  • Western University College of OptometryRecruiting
  • Eye Physicians & Surgeons, PCRecruiting
  • Nova Southeastern University College of Optometry, The Eye InstituteRecruiting
  • Nemours Children's ClinicRecruiting
  • St Luke's HospitalRecruiting
  • Ticho Eye AssociatesRecruiting
  • Ann & Robert H. Lurie Children's Hospital of ChicagoRecruiting
  • Midwestern U Chicago College of OptometryRecruiting
  • Progressive Eye CareRecruiting
  • Indiana School of OptometryRecruiting
  • Indiana University School of OptometryRecruiting
  • Wolfe Eye ClinicRecruiting
  • Wilmer Eye InstituteRecruiting
  • Boston Medical CenterRecruiting
  • Boston Children's Hospital WalthamRecruiting
  • Helen DeVos Children's Hospital Pediatric OphthalmologyRecruiting
  • Mayo ClinicRecruiting
  • PineCone Vision CenterRecruiting
  • Children's Mercy Hospitals and ClinicsRecruiting
  • St. Louis Children's Hospital Eye CenterRecruiting
  • U of MO St. Louis College of OptometryRecruiting
  • University of Nebraska Medical CenterRecruiting
  • Ross Eye Institute, University of Buffalo, Med School Dept OphthalmologyRecruiting
  • State University of New York, College of OptometryRecruiting
  • University of North CarolinaRecruiting
  • Duke University Eye CenterRecruiting
  • Cincinnati Children's HospitalRecruiting
  • Ohio State University College of OptometryRecruiting
  • Dean A. McGee Eye InstituteRecruiting
  • River View Family EyecareRecruiting
  • Pediatric Ophthalmology of ErieRecruiting
  • Conestoga EyeRecruiting
  • Wills Eye HospitalRecruiting
  • Salus University/Pennsylvania College of OptometryRecruiting
  • Southern College of OptometryRecruiting
  • Vanderbilt University Medical Center - Vanderbilt Eye InstituteRecruiting
  • Pediatric Eye Specialists, LLPRecruiting
  • Baylor College of MedicineRecruiting
  • Texas Tech University Health Science CenterRecruiting
  • San Antonio Eye CenterRecruiting
  • University of Incarnate Word Rosenberg School of OptometryRecruiting
  • Rocky Mountain Eye Care AssociatesRecruiting
  • Virginia Pediatric Eye CenterRecruiting
  • Seattle Children's Hospital, University of WashingtonRecruiting
  • Spokane Eye Clinical ResearchRecruiting
  • Snowy Range Vision CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Sequential treatment

Simultaneous treatment

Arm Description

full-time spectacle correction first, with subsequent patching for 2 hours per day/7 days per week only if needed (no improvement (stable/worsening) and residual)

full-time spectacle correction and part-time patching for 2 hours per day/7 days per week

Outcomes

Primary Outcome Measures

Mean Change in Amblyopic Eye logMAR distance Visual Acuity
Amblyopic eye VA (calculated as mean of test and retest) at the last visit that was the basis for a "stable resolved" or "stable residual" determination (in the sequential group, stable residual amblyopia criteria can be reached only after patching has been instituted); or 56-week visit amblyopic-eye VA (calculated as mean of test and retest) in those completing a 56-week visit without ever meeting criteria for "stable resolved" or "stable residual" amblyopia (if retest missing at 56 weeks, the single test value will be used).

Secondary Outcome Measures

Pediatric Eye Questionnaire (PedEyeQ)
Rasch scores for each questionnaire item will be obtained from published look-up tables available at www.pedig.net, and used to calculate a score for each participant and a separate treatment group mean for the three PedEyeQ domains of the Child, Proxy and Parent PedEyeQ at randomization and at each visit. Scores will also be converted to a 0-100 scale to aid in interpretation. Multiplicity adjusted two sided P-values and confidence intervals will be produced. Child PedEyeQ: Functional Vision, Bothered by Eyes and Vision, Social, Frustration / Worry Proxy PedEyeQ: Functional Vision, Bothered by Eyes and Vision, Social, Frustration / Worry, Eyecare Parent PedEyeQ: Impact on Parent and Family, Worry about Child's Eye Condition, Worry about Self-perception and Interactions, Worry about Functional Vision
Proportion Achieving Stable Resolved Outcome with Spectacles Alone
The proportion of participants in the Sequential Spectacles group who achieve "stable resolved" outcome status with spectacles alone will be calculated, along with a multiplicity adjusted two sided P-value and confidence interval.
Proportion of participants who achieve Binary distance visual acuity outcomes
The proportion of participants who achieve the following binary outcomes will be tabulated by treatment group to aid in the interpretation of the primary outcome: The proportion of participants with outcome amblyopic-eye distance VA improvement of ≥ 2 logMAR lines (≥ 10 letters if E-ETDRS) from baseline. The proportion of participants with stable resolved VA. Poisson regression with the log link will be used to estimate the relative risk of each outcome for the sequential versus simultaneous and a multiplicity adjusted two sided P-value and confidence interval. The Poisson models will include an adjustment for baseline amblyopic eye VA. In the event the number of outcomes is too small for reliable estimation with Poisson regression,43 a treatment group difference and 95% confidence interval will be estimated using the Farrington-Manning Score test or other exact method with no adjustment for baseline VA.
Time to Stable Resolved Amblyopia
For those participants who are classified as "stable resolved," the time from baseline to the time meeting that classification will be compared between treatment groups, using a Kaplan-Meier analysis with the logrank test. Multiplicity adjusted two sided P-values and confidence intervals will be produced.
Difference in Mean Change of Distance Visual Acuity after 8 Weeks on Randomized Treatment
An analysis of covariance (ANCOVA) will be performed to compute the difference in mean change in amblyopic-eye distance logMAR VA after 8 weeks between the sequential and simultaneous treatment groups, adjusted for baseline amblyopic eye distance VA, and a multiplicity adjusted two sided P-value and confidence interval will be constructed on the treatment group difference for each time point.
Change in binocularity levels
Binocularity will be assessed on an ordered scale combining the results of the Randot Preschool Test, Randot butterfly, and Worth 4-Dot (W4D) at near. Results of each individual test also will be tabulated at baseline and at the final study visit according to treatment group. The possible levels of binocularity will be 40, 60, 100, 200, 400, 800 seconds of arc (Randot Preschool test), 2000 seconds of arc (Randot butterfly), binocular perception by W4D (4 or 5 lights), or no binocular perception by W4D (2 or 3 lights). This yields an ordered binocularity scale with 9 ordered levels. The change in binocularity levels for each test will be tabulated and compared between treatment groups using the exact Wilcoxon rank-sum test. The proportion of participants in each treatment group unable to perform testing will be tabulated but these participants will not be included in the analysis of change.
Difference in mean change in amblyopic-eye log contrast sensitivity
Contrast sensitivity scores range from unable (<0.90), and then from 0.90 to 2.05 (by 0.05 log contrast sensitivity units). An analysis of covariance (ANCOVA) will be performed to compute the difference in mean change in amblyopic-eye log contrast sensitivity units between the sequential and simultaneous treatment groups, adjusted for baseline amblyopic eye contrast sensitivity, and a multiplicity adjusted two sided P-value and confidence interval will be produced.

Full Information

First Posted
May 5, 2020
Last Updated
February 16, 2023
Sponsor
Jaeb Center for Health Research
Collaborators
National Eye Institute (NEI), Pediatric Eye Disease Investigator Group
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1. Study Identification

Unique Protocol Identification Number
NCT04378790
Brief Title
A Randomized Trial to Evaluate Sequential vs Simultaneous Patching
Acronym
ATS22
Official Title
A Randomized Trial to Evaluate Sequential vs Simultaneous Spectacles Plus Patching for Amblyopia in Children 3 to <13 Years Old
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
December 8, 2020 (Actual)
Primary Completion Date
June 2025 (Anticipated)
Study Completion Date
June 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Jaeb Center for Health Research
Collaborators
National Eye Institute (NEI), Pediatric Eye Disease Investigator Group

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
A randomized trial to determine whether simultaneous treatment with spectacles and patching has an equivalent VA outcome compared with sequential treatment, first with spectacles alone followed by patching (if needed), for previously untreated amblyopia in children 3 to <13 years of age.
Detailed Description
At an enrollment visit, distance VA will be measured in trial frames with or without cycloplegia based on a cycloplegic refraction performed within 30 days. If still apparently eligible, children will be prescribed spectacles and will then return for a spectacle baseline visit, where they will wear their new spectacles for the first time for at least 10 minutes (but no more than 24 hours) and will be tested in those new spectacles to confirm final eligibility prior to randomization. Participants not found to be eligible in their new spectacles will end study participation. Participants eligible for the study will be randomly allocated to one of two treatment groups: Sequential (spectacles alone) and then patching if needed (monitored by ODM), or Simultaneous (spectacles and patching monitored by ODM). After randomization, follow-up visits will occur at 8-week intervals through 56 weeks. At each visit on or after the 8-week visit, participants will be classified as either: stable/worsening or improving; those stable/worsening are then classified as having either resolved or residual amblyopia, provided that the current and most recent previous visit were completed at least 6-weeks apart (target 8 weeks) and provided the required test and retest VA testing was completed. Participants who are stable/worsening and have residual amblyopia in the sequential group will start patching (monitored by ODM) and continue to be followed every 8 weeks. Participants in the simultaneous group, or in the sequential group after having advanced to patching, who are stable/worsening but have residual amblyopia will be released to treatment at investigator discretion. All participants continue 8-weekly visits until 56 weeks when Study participation ends.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Amblyopia
Keywords
patching, glasses, spectacles, simultaneous, sequential

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
544 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Sequential treatment
Arm Type
Active Comparator
Arm Description
full-time spectacle correction first, with subsequent patching for 2 hours per day/7 days per week only if needed (no improvement (stable/worsening) and residual)
Arm Title
Simultaneous treatment
Arm Type
Experimental
Arm Description
full-time spectacle correction and part-time patching for 2 hours per day/7 days per week
Intervention Type
Other
Intervention Name(s)
Patching
Other Intervention Name(s)
Eye Patch
Intervention Description
Procedure in which the eye is covered utilizing a patch to increase the strength of the uncovered eye.
Intervention Type
Other
Intervention Name(s)
Glasses
Other Intervention Name(s)
Spectacles
Intervention Description
Eye Glasses are created and worn by patient to improve vision
Primary Outcome Measure Information:
Title
Mean Change in Amblyopic Eye logMAR distance Visual Acuity
Description
Amblyopic eye VA (calculated as mean of test and retest) at the last visit that was the basis for a "stable resolved" or "stable residual" determination (in the sequential group, stable residual amblyopia criteria can be reached only after patching has been instituted); or 56-week visit amblyopic-eye VA (calculated as mean of test and retest) in those completing a 56-week visit without ever meeting criteria for "stable resolved" or "stable residual" amblyopia (if retest missing at 56 weeks, the single test value will be used).
Time Frame
56 weeks
Secondary Outcome Measure Information:
Title
Pediatric Eye Questionnaire (PedEyeQ)
Description
Rasch scores for each questionnaire item will be obtained from published look-up tables available at www.pedig.net, and used to calculate a score for each participant and a separate treatment group mean for the three PedEyeQ domains of the Child, Proxy and Parent PedEyeQ at randomization and at each visit. Scores will also be converted to a 0-100 scale to aid in interpretation. Multiplicity adjusted two sided P-values and confidence intervals will be produced. Child PedEyeQ: Functional Vision, Bothered by Eyes and Vision, Social, Frustration / Worry Proxy PedEyeQ: Functional Vision, Bothered by Eyes and Vision, Social, Frustration / Worry, Eyecare Parent PedEyeQ: Impact on Parent and Family, Worry about Child's Eye Condition, Worry about Self-perception and Interactions, Worry about Functional Vision
Time Frame
56 weeks
Title
Proportion Achieving Stable Resolved Outcome with Spectacles Alone
Description
The proportion of participants in the Sequential Spectacles group who achieve "stable resolved" outcome status with spectacles alone will be calculated, along with a multiplicity adjusted two sided P-value and confidence interval.
Time Frame
56 Weeks
Title
Proportion of participants who achieve Binary distance visual acuity outcomes
Description
The proportion of participants who achieve the following binary outcomes will be tabulated by treatment group to aid in the interpretation of the primary outcome: The proportion of participants with outcome amblyopic-eye distance VA improvement of ≥ 2 logMAR lines (≥ 10 letters if E-ETDRS) from baseline. The proportion of participants with stable resolved VA. Poisson regression with the log link will be used to estimate the relative risk of each outcome for the sequential versus simultaneous and a multiplicity adjusted two sided P-value and confidence interval. The Poisson models will include an adjustment for baseline amblyopic eye VA. In the event the number of outcomes is too small for reliable estimation with Poisson regression,43 a treatment group difference and 95% confidence interval will be estimated using the Farrington-Manning Score test or other exact method with no adjustment for baseline VA.
Time Frame
56 weeks
Title
Time to Stable Resolved Amblyopia
Description
For those participants who are classified as "stable resolved," the time from baseline to the time meeting that classification will be compared between treatment groups, using a Kaplan-Meier analysis with the logrank test. Multiplicity adjusted two sided P-values and confidence intervals will be produced.
Time Frame
56 weeks
Title
Difference in Mean Change of Distance Visual Acuity after 8 Weeks on Randomized Treatment
Description
An analysis of covariance (ANCOVA) will be performed to compute the difference in mean change in amblyopic-eye distance logMAR VA after 8 weeks between the sequential and simultaneous treatment groups, adjusted for baseline amblyopic eye distance VA, and a multiplicity adjusted two sided P-value and confidence interval will be constructed on the treatment group difference for each time point.
Time Frame
56 Weeks
Title
Change in binocularity levels
Description
Binocularity will be assessed on an ordered scale combining the results of the Randot Preschool Test, Randot butterfly, and Worth 4-Dot (W4D) at near. Results of each individual test also will be tabulated at baseline and at the final study visit according to treatment group. The possible levels of binocularity will be 40, 60, 100, 200, 400, 800 seconds of arc (Randot Preschool test), 2000 seconds of arc (Randot butterfly), binocular perception by W4D (4 or 5 lights), or no binocular perception by W4D (2 or 3 lights). This yields an ordered binocularity scale with 9 ordered levels. The change in binocularity levels for each test will be tabulated and compared between treatment groups using the exact Wilcoxon rank-sum test. The proportion of participants in each treatment group unable to perform testing will be tabulated but these participants will not be included in the analysis of change.
Time Frame
56 Weeks
Title
Difference in mean change in amblyopic-eye log contrast sensitivity
Description
Contrast sensitivity scores range from unable (<0.90), and then from 0.90 to 2.05 (by 0.05 log contrast sensitivity units). An analysis of covariance (ANCOVA) will be performed to compute the difference in mean change in amblyopic-eye log contrast sensitivity units between the sequential and simultaneous treatment groups, adjusted for baseline amblyopic eye contrast sensitivity, and a multiplicity adjusted two sided P-value and confidence interval will be produced.
Time Frame
56 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
3 Years
Maximum Age & Unit of Time
13 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 3 to <13 years at the time of randomization Amblyopia associated with anisometropia, strabismus, or both o Criteria for strabismic amblyopia: At least one of the following must be met: Presence of a heterotropia on examination at distance or near fixation (with or without optical correction) Documented history of strabismus which is no longer present (which in the judgment of the investigator could have caused amblyopia) Criteria for anisometropia: At least one of the following criteria must be met: 1.00 D difference between eyes in spherical equivalent (SE) 1.50 D difference in astigmatism between corresponding meridians in the two eyes Criteria for combined-mechanism amblyopia: Both of the following criteria must be met: Criteria for strabismus are met (see above) 1.00 D difference between eyes in spherical equivalent OR ≥1.50 D difference in astigmatism between corresponding meridians in the two eyes No previous treatment for amblyopia, including no more than 24 hours of spectacle wear. Investigator planning to initiate spectacle correction of refractive error meeting the following criteria based on a cycloplegic refraction that has been performed within 30 days: Full correction of anisometropia Full correction of astigmatism with the same axis found by the cycloplegic refraction Full correction of any myopia Hyperopia must not be under corrected by more than 1.50 D, and reduction in plus sphere must be symmetric in the two eyes. At enrollment, single VA measured in each eye assessed in trial frames with the spectacle correction the investigator plans to prescribe, using the investigator's routine method as follows: VA in the amblyopic eye 20/40 to 20/200 inclusive. Age-normal VA in the fellow eye:40,41 3 years: 0.4 logMAR (20/50) or better 4 years: 0.3 logMAR (20/40) or better 5-6 years: 0.2 logMAR (20/32) or better 7-12 years: 0.12 logMAR (78 letters) or better Interocular difference ≥ 3 logMAR lines (0.3 logMAR) or ≥ 15 letters o When participants return for the Spectacle Baseline / Randomization Visit with their new spectacles, they will need to meet the same criteria as above using the ATS-HOTV or E-ETDRS protocol after wearing the new spectacles for at least 10 minutes (based upon the mean of a test and retest of VA in those new spectacles). Investigator is willing to prescribe spectacle wear followed sequentially by patching or simultaneous spectacles and patching treatment per protocol. Parent understands the protocol and is willing to accept randomization. Parent has phone (or access to phone) and is willing to be contacted by Jaeb Center staff or other study staff. Relocation outside of area of an active PEDIG site for this study within the next 56 weeks is not anticipated. Exclusion Criteria: Myopia greater than -6.00 D spherical equivalent in either eye. Previous intraocular or refractive surgery. Planned strabismus surgery in the next 56 weeks. Any previous treatment for amblyopia (patching, atropine, Bangerter filter, vision therapy, or binocular treatment). Previous spectacle or contact lens wear for more than 24 hours. Parent and participant willing to forego option of contact lens wear for the duration of the study. Ocular co-morbidity that may reduce VA determined by an ocular examination performed within the past 7 months (Note: nystagmus per se does not exclude the participant if the above VA criteria are met). Severe developmental delay that would interfere with treatment or evaluation (in the opinion of the investigator). Participants with mild speech delay or reading and/or learning disabilities or attention deficit hyperactivity disorder (ADHD) are not excluded. Known allergy to adhesive patches. Known allergy to silicone.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Raymond T Kraker, MSPH
Phone
813-975-8690
Email
rkraker@jaeb.org
First Name & Middle Initial & Last Name or Official Title & Degree
Brooke P Fimbel
Phone
813-975-8690
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Vivian Manh
Organizational Affiliation
Seattle Children's Hospital, University of Washington
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Michael Gray
Organizational Affiliation
Children's Hospital Medical Center, Cincinnati
Official's Role
Study Chair
Facility Information:
Facility Name
University of Alabama at Birmingham
City
Birmingham
State/Province
Alabama
ZIP/Postal Code
35294
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Katherine Weise, OD, MBA
Phone
205-934-6739
Email
kweise@uab.edu
Facility Name
Midwestern University Eye Institute
City
Glendale
State/Province
Arizona
ZIP/Postal Code
85308
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Alicia Feis, OD
Phone
623-806-7271
Email
afeis@midwestern.edu
First Name & Middle Initial & Last Name & Degree
Christina A Esposito, OD
Facility Name
University of Arizona
City
Tucson
State/Province
Arizona
ZIP/Postal Code
85711
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jonathan M Holmes, MD
Phone
520-321-3677
Email
jmholmes@arizona.edu
Facility Name
Marshall B. Ketchum University
City
Fullerton
State/Province
California
ZIP/Postal Code
92831
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Angela Chen, O.D., M.S.
Phone
714-449-7432
Email
angelachen@ketchum.edu
First Name & Middle Initial & Last Name & Degree
Angela Chen, O.D., M.S.
Facility Name
Loma Linda University Health Care, Dept. of Ophthalmology
City
Loma Linda
State/Province
California
ZIP/Postal Code
92354
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Timothy Winter, M.D.
Phone
909-558-2168
Email
twwinter@llu.edu
Facility Name
Stanford University
City
Palo Alto
State/Province
California
ZIP/Postal Code
94303
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Tawna L Roberts, OD
Phone
650-724-7115
Email
tawnar@stanford.edu
Facility Name
Western University College of Optometry
City
Pomona
State/Province
California
ZIP/Postal Code
91766
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ida Chung, OD
Phone
909-469-8687
Email
ichung@westernu.edu
Facility Name
Eye Physicians & Surgeons, PC
City
Milford
State/Province
Connecticut
ZIP/Postal Code
06460
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jennifer A Galvin, MD
Phone
203-795-0766
Email
jennygalvin@gmail.com
Facility Name
Nova Southeastern University College of Optometry, The Eye Institute
City
Fort Lauderdale
State/Province
Florida
ZIP/Postal Code
33382
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Micheal Au, OD
Phone
954-262-1426
Email
michau@nova.edu
Facility Name
Nemours Children's Clinic
City
Jacksonville
State/Province
Florida
ZIP/Postal Code
32207
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
John Erickson, OD
Phone
904-697-3775
Email
john.erickson@nemours.org
Facility Name
St Luke's Hospital
City
Boise
State/Province
Idaho
ZIP/Postal Code
83702
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Katherine Lee, MD
Phone
208-381-6910
Email
leek@slhs.org
Facility Name
Ticho Eye Associates
City
Chicago Ridge
State/Province
Illinois
ZIP/Postal Code
60415
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Benjamin Ticho
Phone
708-423-4070
Email
Bticho@mac.com
Facility Name
Ann & Robert H. Lurie Children's Hospital of Chicago
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60611
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Bahram Rahmani, MD
Phone
312-227-6189
Email
BRahmani@luriechildrens.org
Facility Name
Midwestern U Chicago College of Optometry
City
Downers Grove
State/Province
Illinois
ZIP/Postal Code
60515
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Samantha Rice, O.D
Phone
630-743-4500
Email
srice@midwestern.edu
Facility Name
Progressive Eye Care
City
Lisle
State/Province
Illinois
ZIP/Postal Code
60532
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Patricia Davis, M.D.
Phone
630-245-0989
Email
idocmd@comcast.net
Facility Name
Indiana School of Optometry
City
Bloomington
State/Province
Indiana
ZIP/Postal Code
47405
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Don W. Lyon, O.D.
Phone
317-856-1964
Email
dwlyon@Indiana.edu
First Name & Middle Initial & Last Name & Degree
Don W. Lyon, O.D.
Facility Name
Indiana University School of Optometry
City
Indianapolis
State/Province
Indiana
ZIP/Postal Code
47405
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kathryn M Haider, MD
Phone
317-944-8103
Email
khaider@iupui.edu
First Name & Middle Initial & Last Name & Degree
Kathyrn M Haider, MD
First Name & Middle Initial & Last Name & Degree
Heather A Smith, MD
First Name & Middle Initial & Last Name & Degree
Charline S Boente, MD
First Name & Middle Initial & Last Name & Degree
David K Wallace, MD
Facility Name
Wolfe Eye Clinic
City
West Des Moines
State/Province
Iowa
ZIP/Postal Code
50266
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Derek Bitner, MD
Phone
800-542-7957
Email
dbitner@wolfeclinic.com
Facility Name
Wilmer Eye Institute
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21287-9028
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Michael X Repka, MD
Phone
410-955-8314
Email
mrepka@jhmi.edu
Facility Name
Boston Medical Center
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02118
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Stephen Christiansen, MD
Phone
617-414-2020
Email
spchris@bu.edu
Facility Name
Boston Children's Hospital Waltham
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02453
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Aparna Raghuram, O.D., Ph.D.
Phone
617-355-6401
Email
aparna.raghuram@childrens.harvard.edu
Facility Name
Helen DeVos Children's Hospital Pediatric Ophthalmology
City
Grand Rapids
State/Province
Michigan
ZIP/Postal Code
49503
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Brooke Geddie, DO
Phone
616-267-2605
Email
brooke.geddie@helendevoschildrens.org
Facility Name
Mayo Clinic
City
Rochester
State/Province
Minnesota
ZIP/Postal Code
55905
Country
United States
Individual Site Status
Recruiting
Facility Name
PineCone Vision Center
City
Sartell
State/Province
Minnesota
ZIP/Postal Code
56377
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kevy M Simmons, OD
Phone
320-258-3915
Email
ksimmons@pineconevisioncenter.com
Facility Name
Children's Mercy Hospitals and Clinics
City
Kansas City
State/Province
Missouri
ZIP/Postal Code
64108
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jennifer Qayum, MD
Phone
816-701-1337
Email
jvqayum@cmh.edu
Facility Name
St. Louis Children's Hospital Eye Center
City
Saint Louis
State/Province
Missouri
ZIP/Postal Code
63110
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Margaret M Reynolds, MD
Phone
314-454-6026
Email
margaret.reynolds@wustl.edu
Facility Name
U of MO St. Louis College of Optometry
City
Saint Louis
State/Province
Missouri
ZIP/Postal Code
63121
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Erin Brooks
Phone
314-516-5808
Email
brooksem@umsl.edu
Facility Name
University of Nebraska Medical Center
City
Omaha
State/Province
Nebraska
ZIP/Postal Code
68114
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Donny Suh, MD
Phone
402-559-2977
Email
dsuh@childrensomaha.org
Facility Name
Ross Eye Institute, University of Buffalo, Med School Dept Ophthalmology
City
Buffalo
State/Province
New York
ZIP/Postal Code
14209
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
John H Lillvis, MD PhD
Phone
716-881-7900
Email
jhlillvi@buffalo.edu
Facility Name
State University of New York, College of Optometry
City
New York
State/Province
New York
ZIP/Postal Code
10036
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marilyn Vricella, OD
Phone
212-780-5182
Email
mvricella@sunyopt.edu
Facility Name
University of North Carolina
City
Chapel Hill
State/Province
North Carolina
ZIP/Postal Code
27599
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Katherine O Whitfield, MD
Phone
919-966-5296
Email
katherine_whitfield@med.unc.edu
Facility Name
Duke University Eye Center
City
Durham
State/Province
North Carolina
ZIP/Postal Code
27710
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Laura Enyedi, MD
Phone
919-684-2038
Email
enyed001@mc.duke.edu
Facility Name
Cincinnati Children's Hospital
City
Cincinnati
State/Province
Ohio
ZIP/Postal Code
45229
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Michael Gray, MD
Phone
513-636-4751
Email
Michael.Gray@cchmc.org
Facility Name
Ohio State University College of Optometry
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43210-1280
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marjean T Kulp, O.D.
Phone
614-688-3336
Email
mtkulp@optometry.ohio-state.edu
First Name & Middle Initial & Last Name & Degree
Marjean T Kulp, O.D.
Facility Name
Dean A. McGee Eye Institute
City
Oklahoma City
State/Province
Oklahoma
ZIP/Postal Code
73104
Country
United States
Individual Site Status
Recruiting
Facility Name
River View Family Eyecare
City
Albany
State/Province
Oregon
ZIP/Postal Code
97321
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Aaron D Salzano, OD
Phone
541-967-3097
Email
aaron.salzano@gmail.com
Facility Name
Pediatric Ophthalmology of Erie
City
Erie
State/Province
Pennsylvania
ZIP/Postal Code
16501
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Nicholas A Sala, D.O.
Phone
814-454-6307
Email
nasala@kidseyeserie.com
Facility Name
Conestoga Eye
City
Lancaster
State/Province
Pennsylvania
ZIP/Postal Code
17601
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
David Silbert, MD
Phone
717-541-9700
Email
davidsilbertmd@gmail.com
Facility Name
Wills Eye Hospital
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19107
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kammi B Gunton, MD
Phone
215-928-3914
Email
kbgunton@comcast.net
Facility Name
Salus University/Pennsylvania College of Optometry
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19141
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Erin Jenewein, OD
Phone
215-276-6000
Email
Ejenewein@salus.edu
Facility Name
Southern College of Optometry
City
Memphis
State/Province
Tennessee
ZIP/Postal Code
38104
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marie Bodack, OD
Phone
901-722-3276
Email
mbodack@sco.edu
Facility Name
Vanderbilt University Medical Center - Vanderbilt Eye Institute
City
Nashville
State/Province
Tennessee
ZIP/Postal Code
37232
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lori Ann Kehler, OD
Phone
615-936-2020
Email
lori.kehler@vanderbilt.edu
Facility Name
Pediatric Eye Specialists, LLP
City
Fort Worth
State/Province
Texas
ZIP/Postal Code
76014
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Michael G Hunt, MD
Facility Name
Baylor College of Medicine
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Irene T Tung, MD
Phone
832-822-3230
Facility Name
Texas Tech University Health Science Center
City
Lubbock
State/Province
Texas
ZIP/Postal Code
79430
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lingkun Kong
Phone
832-283-1577
Email
lxxkong@gmail.com
Facility Name
San Antonio Eye Center
City
San Antonio
State/Province
Texas
ZIP/Postal Code
78215
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
manpreet Chhabra
Phone
210-226-6169
Ext
1005
Email
manpreetch@gmail.com
Facility Name
University of Incarnate Word Rosenberg School of Optometry
City
San Antonio
State/Province
Texas
ZIP/Postal Code
78229
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Aubrey D Breithaupt, OD
Phone
210-283-6881
Email
breithau@uiwtx.edu
Facility Name
Rocky Mountain Eye Care Associates
City
Salt Lake City
State/Province
Utah
ZIP/Postal Code
84107
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
David Petersen, MD
Phone
801-264-4450
Email
DPetersen@RMEyecare.com
First Name & Middle Initial & Last Name & Degree
David Petersen, MD
Facility Name
Virginia Pediatric Eye Center
City
Norfolk
State/Province
Virginia
ZIP/Postal Code
23502
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Eric Crouch, MD
Phone
757-461-0050
Email
ercrouch@gmail.com
Facility Name
Seattle Children's Hospital, University of Washington
City
Seattle
State/Province
Washington
ZIP/Postal Code
98105
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Vivian Manh, O.D., M.S.
Phone
206-987-4950
Email
vmanh@uw.edu
First Name & Middle Initial & Last Name & Degree
Vivian Manh, O.D., M.S>
Facility Name
Spokane Eye Clinical Research
City
Spokane
State/Province
Washington
ZIP/Postal Code
99204
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jeffrey Colburn
Phone
509-456-0107
Email
jcolburn@spokaneeye.com
Facility Name
Snowy Range Vision Center
City
Laramie
State/Province
Wyoming
ZIP/Postal Code
82070
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Amy Aldrich
Phone
307-742-2020
Email
aldrich@snowyrangevision.com

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
In accordance with the NIH data sharing policy, a de-identified database is placed in the public domain on the Pediatric Eye Disease Investigator Group (PEDIG) public website after the completion of each protocol and publication of the primary manuscript.
IPD Sharing Time Frame
Data will be made available after publication.
IPD Sharing Access Criteria
Users accessing the data must enter an email address.
IPD Sharing URL
http://pedig.jaeb.org

Learn more about this trial

A Randomized Trial to Evaluate Sequential vs Simultaneous Patching

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