Cataract DME - Peri vs. Intraop
Primary Purpose
Diabetic Macular Edema, Cataract
Status
Withdrawn
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Aflibercept injected Pre- and Post-operatively
Aflibercept injected intraoperatively
Sponsored by
About this trial
This is an interventional treatment trial for Diabetic Macular Edema focused on measuring anti-VEGF injections, pre-existing DME, cataract surgery
Eligibility Criteria
Inclusion Criteria:
- Adults over age 18 with diabetes mellitus, diabetic macular edema and visually significant cataracts planning to undergo cataract surgery
Exclusion Criteria:
- Patients who have undergone panretinal photocoagulation (PRP) in prior 4 months or an ocular condition (other than cataract and DME) that might affect visual acuity during course of study.
- Patients with history of vitrectomy.
- Patients with neovascular glaucoma.
Sites / Locations
- Emory Clinic
- Grady Health System
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Aflibercept injected Pre- and Post-operatively
Aflibercept injected intraoperatively
Arm Description
Pre- and Post-operative time of Aflibercept injections
Intraoperative time of Aflibercept injection
Outcomes
Primary Outcome Measures
Change in best-corrected visual acuity (BCVA)
BCVA is a measurement of the best vision correction that can be achieved, such as glasses, as measured on the standard Snellen eye chart. For example, if uncorrected eyesight is 20/200, but patient can see 20/20 with glasses, the BCVA is 20/20.
Secondary Outcome Measures
Change in optical coherence tomography (OCT) central subfield (CSF) thickness
Optical coherence tomography (OCT) is an important imaging modality in the evaluation and management of retinal diseases. Change in central subfield (CSF) thickness will be measured and recorded.
Total number of postoperative injections
Total number of postoperative injections will be calculated
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03920878
Brief Title
Cataract DME - Peri vs. Intraop
Official Title
Peri- Versus Intra-operative Anti-vascular Endothelial Growth Factor Intravitreous Injections for Diabetic Macular Edema in Patients Undergoing Cataract Surgery
Study Type
Interventional
2. Study Status
Record Verification Date
December 2020
Overall Recruitment Status
Withdrawn
Why Stopped
The study team was unable to secure sufficient funding and administrative support.
Study Start Date
May 2020 (Anticipated)
Primary Completion Date
June 2020 (Anticipated)
Study Completion Date
June 2020 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Emory University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Goals of the study are to evaluate how peri-operative versus intra-operative anti-VEGF intravitreous injections affect visual acuity (BCVA) in patients with persistent diabetic macular edema who are undergoing cataract surgery; and to evaluate how peri-operative versus intra-operative anti-VEGF intravitreous injections affect OCT CSF thickness and total number of postoperative injections in patients with diabetic macular edema who are undergoing cataract surgery.
Detailed Description
Along with age, diabetes is a major risk factor for cataract formation, which can lead to significant vision loss and disability without medical intervention. Unfortunately, diabetic patients, particularly those with diabetic macular edema (DME), experience poorer visual outcomes after undergoing cataract surgery compared to non-diabetics. Reasons for this is multifactorial but includes an increased risk in the development of post-operative cystoid macular edema, and exacerbation of baseline DME. This poses a significant challenge in managing concomitant DME and visually-significant cataracts.
Goals of the study are to evaluate how peri-operative versus intra-operative anti-VEGF intravitreous injections affect visual acuity (BCVA) in patients with persistent diabetic macular edema who are undergoing cataract surgery; and to evaluate how peri-operative versus intra-operative anti-VEGF intravitreous injections affect OCT CSF thickness and total number of postoperative injections in patients with diabetic macular edema who are undergoing cataract surgery.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetic Macular Edema, Cataract
Keywords
anti-VEGF injections, pre-existing DME, cataract surgery
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Aflibercept injected Pre- and Post-operatively
Arm Type
Experimental
Arm Description
Pre- and Post-operative time of Aflibercept injections
Arm Title
Aflibercept injected intraoperatively
Arm Type
Active Comparator
Arm Description
Intraoperative time of Aflibercept injection
Intervention Type
Drug
Intervention Name(s)
Aflibercept injected Pre- and Post-operatively
Other Intervention Name(s)
EYELEA
Intervention Description
Three injections of aflibercept before cataract surgery, and aflibercept injections after surgery within 14-21 days of the day of surgery (number of injections depends on clinical exam findings, visual acuity and retinal thickness).
Intervention Type
Drug
Intervention Name(s)
Aflibercept injected intraoperatively
Other Intervention Name(s)
EYELEA
Intervention Description
Three injections of aflibercept before surgery and one injection of aflibercept during the course of the surgery by cataract surgeon.
Primary Outcome Measure Information:
Title
Change in best-corrected visual acuity (BCVA)
Description
BCVA is a measurement of the best vision correction that can be achieved, such as glasses, as measured on the standard Snellen eye chart. For example, if uncorrected eyesight is 20/200, but patient can see 20/20 with glasses, the BCVA is 20/20.
Time Frame
1 month, 3 months and 6 months after cataract surgery
Secondary Outcome Measure Information:
Title
Change in optical coherence tomography (OCT) central subfield (CSF) thickness
Description
Optical coherence tomography (OCT) is an important imaging modality in the evaluation and management of retinal diseases. Change in central subfield (CSF) thickness will be measured and recorded.
Time Frame
24 hours post-operatively, 1 month, 3 months and 6 months after cataract surgery
Title
Total number of postoperative injections
Description
Total number of postoperative injections will be calculated
Time Frame
6 months after cataract surgery
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Adults over age 18 with diabetes mellitus, diabetic macular edema and visually significant cataracts planning to undergo cataract surgery
Exclusion Criteria:
Patients who have undergone panretinal photocoagulation (PRP) in prior 4 months or an ocular condition (other than cataract and DME) that might affect visual acuity during course of study.
Patients with history of vitrectomy.
Patients with neovascular glaucoma.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Andrew Hendrick, MD
Organizational Affiliation
Emory University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Emory Clinic
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30322
Country
United States
Facility Name
Grady Health System
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30322
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
No individual de-identified participant data (including data dictionaries) will be shared. Only composite results with publication will be shared.
Learn more about this trial
Cataract DME - Peri vs. Intraop
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