Refitting Daily Disposable Contact Lens Wearers With Dry Eye Disease With A Different Daily Disposable Lens Type (CORGI)
Primary Purpose
Dry Eye
Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Delfilcon A
Sponsored by
About this trial
This is an interventional basic science trial for Dry Eye
Eligibility Criteria
Inclusion Criteria:
- Is at least 17 years of age and has full legal capacity to volunteer;
- Has read and signed an information consent letter;
- Is willing and able to follow instructions and maintain the appointment schedule;
As per TFOS DEWS II, have dry eye symptoms (without CL wear) as determined by an OSDI score of ≥13 and at least one of the following:
- Tear osmolarity ≥ 308mOsm/L or interocular difference >8 mOsm/L
- Non-invasive tear breakup time of < 10 seconds in at least one eye
- More than 5 spots of corneal staining OR > 9 conjunctival spots in at least one eye
- Reports dryness while wearing DD CLs with CLDEQ-8 score ≥ 12 and ≤ 203
- Habitually wears soft spherical DD CLs with a power between +6.00D and -10.00D
- Manifest spectacle cyl ≤1.00DC in either eye
- BCVA ≤0.20 log MAR each eye with habitual & DT1
- Acceptable fit with habitual & DT1
- Willing to wear DT1 CLs at least 3 days per week and 6 hours per day throughout the study
Exclusion Criteria:
- Is participating in any concurrent clinical or research study;
- Has any known active* ocular disease and/or infection;
- Has a systemic condition that in the opinion of the investigator may affect a study outcome variable;
- Is using any systemic or topical medications that in the opinion of the investigator may affect a study outcome variable;
- Has known sensitivity to the diagnostic pharmaceuticals to be used in the study;
- Is pregnant, lactating or planning a pregnancy at the time of enrolment (by self-report);
- Is aphakic;
- Has undergone refractive error surgery;
- Has taken part in another clinical research study within the last 14 days;
- Current habitual wearer of DT1
Any ocular and/or systemic conditions or concomitant medication to contraindicate contact lens wear or be expected to interfere with the primary outcome variables.
- For the purposes of this study, active ocular disease is defined as infection or inflammation which requires therapeutic treatment. Mild (i.e. not considered clinically relevant) lid abnormalities (blepharitis, meibomian gland dysfunction, papillae), corneal and conjunctival staining and dry eye are not considered active ocular disease. Neovascularization and corneal scars are the result of previous hypoxia, infection or inflammation and are therefore not active.
Sites / Locations
- Centre for Ocular Research & Education
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Delfilcon A
Arm Description
All study participants will be refit with Delfilcon A (Dailies Total 1) lenses which they will wear for 1 month.
Outcomes
Primary Outcome Measures
Subjective Comfort at End of Day With Contact Lens Wear
Participants rate their end of day comfort on a scale from 0 (worst) to 100 (best).
Subjective Comfort at End of Day With Contact Lens Wear
Participants rate their end of day comfort on a scale from 0 (worst) to 100 (best).
Subjective Comfort at End of Day With Contact Lens Wear
Participants rate their end of day comfort on a scale from 0 (worst) to 100 (best).
Subjective Comfort at End of Day With Contact Lens Wear
Participants rate their end of day comfort on a scale from 0 (worst) to 100 (best).
Subjective Comfort at End of Day With Contact Lens Wear
Participants rate their end of day comfort on a scale from 0 (worst) to 100 (best).
Subjective Comfort at End of Day With Contact Lens Wear
Participants rate their end of day comfort on a scale from 0 (worst) to 100 (best).
Subjective Comfort at End of Day With Contact Lens Wear
Participants rate their end of day comfort on a scale from 0 (worst) to 100 (best).
Subjective Comfort at End of Day With Contact Lens Wear
Participants rate their end of day comfort on a scale from 0 (worst) to 100 (best).
Subjective Comfort at End of Day With Contact Lens Wear
Participants rate their end of day comfort on a scale from 0 (worst) to 100 (best).
Subjective Comfort at End of Day With Contact Lens Wear
Participants rate their end of day comfort on a scale from 0 (worst) to 100 (best).
Subjective Comfort at End of Day With Contact Lens Wear
Participants rate their end of day comfort on a scale from 0 (worst) to 100 (best).
Subjective Rating of End of Day Dryness With Contact Lens Wear
Participants rate their end of day dryness on a scale from 0 (worst) to 100 (best).
Subjective Rating of End of Day Dryness With Contact Lens Wear
Participants rate their end of day dryness on a scale from 0 (worst) to 100 (best).
Subjective Rating of End of Day Dryness With Contact Lens Wear
Participants rate their end of day dryness on a scale from 0 (worst) to 100 (best).
Subjective Rating of End of Day Dryness With Contact Lens Wear
Participants rate their end of day dryness on a scale from 0 (worst) to 100 (best).
Subjective Rating of End of Day Dryness With Contact Lens Wear
Participants rate their end of day dryness on a scale from 0 (worst) to 100 (best).
Subjective Rating of End of Day Dryness With Contact Lens Wear
Participants rate their end of day dryness on a scale from 0 (worst) to 100 (best).
Subjective Rating of End of Day Dryness With Contact Lens Wear
Participants rate their end of day dryness on a scale from 0 (worst) to 100 (best).
Subjective Rating of End of Day Dryness With Contact Lens Wear
Participants rate their end of day dryness on a scale from 0 (worst) to 100 (best).
Subjective Rating of End of Day Dryness With Contact Lens Wear
Participants rate their end of day dryness on a scale from 0 (worst) to 100 (best).
Subjective Rating of End of Day Dryness With Contact Lens Wear
Participants rate their end of day dryness on a scale from 0 (worst) to 100 (best).
Subjective Rating of End of Day Dryness With Contact Lens Wear
Participants rate their end of day dryness on a scale from 0 (worst) to 100 (best).
Average Lens Wear Time
Average lens wear time is recorded
Average Lens Wear Time
Average lens wear time is recorded
Average Lens Wear Time
Average lens wear time is recorded
Average Lens Wear Time
Average lens wear time is recorded
Average Lens Wear Time
Average lens wear time is recorded
Average Lens Wear Time
Average lens wear time is recorded
Average Lens Wear Time
Average lens wear time is recorded
Average Lens Wear Time
Average lens wear time is recorded
Average Lens Wear Time
Average lens wear time is recorded
Average Lens Wear Time
Average lens wear time is recorded
Average Lens Wear Time
Average lens wear time is recorded
Comfortable Lens Wear Time
Comfortable lens wear time (Time of discomfort - Time of insertion)
Comfortable Lens Wear Time
Comfortable lens wear time (Time of discomfort - Time of insertion)
Comfortable Lens Wear Time
Comfortable lens wear time (Time of discomfort - Time of insertion)
Comfortable Lens Wear Time
Comfortable lens wear time (Time of discomfort - Time of insertion)
Comfortable Lens Wear Time
Comfortable lens wear time (Time of discomfort - Time of insertion)
Comfortable Lens Wear Time
Comfortable lens wear time (Time of discomfort - Time of insertion)
Comfortable Lens Wear Time
Comfortable lens wear time (Time of discomfort - Time of insertion)
Comfortable Lens Wear Time
Comfortable lens wear time (Time of discomfort - Time of insertion)
Comfortable Lens Wear Time
Comfortable lens wear time (Time of discomfort - Time of insertion)
Comfortable Lens Wear Time
Comfortable lens wear time (Time of discomfort - Time of insertion)
Comfortable Lens Wear Time
Comfortable lens wear time (Time of discomfort - Time of insertion)
Secondary Outcome Measures
Full Information
NCT ID
NCT04105842
First Posted
September 13, 2019
Last Updated
July 13, 2023
Sponsor
University of Waterloo
Collaborators
Alcon Research
1. Study Identification
Unique Protocol Identification Number
NCT04105842
Brief Title
Refitting Daily Disposable Contact Lens Wearers With Dry Eye Disease With A Different Daily Disposable Lens Type
Acronym
CORGI
Official Title
Refitting Daily Disposable Contact Lens Wearers With Dry Eye Disease With A Different Daily Disposable Lens Type
Study Type
Interventional
2. Study Status
Record Verification Date
June 2023
Overall Recruitment Status
Completed
Study Start Date
September 23, 2019 (Actual)
Primary Completion Date
July 28, 2022 (Actual)
Study Completion Date
July 28, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Waterloo
Collaborators
Alcon Research
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to refit habitual wearers of daily disposable contact lenses who currently experience symptoms of dry eye and discomfort during lens wear with a different type of daily disposable contact lens. Ocular signs and symptoms of dry eye will be assessed following the guidelines outlined by the Tear Film and Ocular Surface Society (TFOS) in the Dry Eye Workshop II (DEWS II). The performance of the habitual contact lenses and the study lenses will be determined using different optometric assessments. Study lenses will be worn for one month following a daily disposable wear schedule.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dry Eye
7. Study Design
Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Masking Description
Participants will be masked to the lens type (brand) they will be wearing during the study in order to reduce bias towards or against this product
Allocation
N/A
Enrollment
40 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Delfilcon A
Arm Type
Experimental
Arm Description
All study participants will be refit with Delfilcon A (Dailies Total 1) lenses which they will wear for 1 month.
Intervention Type
Device
Intervention Name(s)
Delfilcon A
Other Intervention Name(s)
Dailies Total 1
Intervention Description
Participants wear delafilcon A contact lenses on a daily disposable basis.
Primary Outcome Measure Information:
Title
Subjective Comfort at End of Day With Contact Lens Wear
Description
Participants rate their end of day comfort on a scale from 0 (worst) to 100 (best).
Time Frame
Day 1 after screening with habitual lenses
Title
Subjective Comfort at End of Day With Contact Lens Wear
Description
Participants rate their end of day comfort on a scale from 0 (worst) to 100 (best).
Time Frame
Day 3 after screening with habitual lenses
Title
Subjective Comfort at End of Day With Contact Lens Wear
Description
Participants rate their end of day comfort on a scale from 0 (worst) to 100 (best).
Time Frame
Day 5 after screening with habitual lenses
Title
Subjective Comfort at End of Day With Contact Lens Wear
Description
Participants rate their end of day comfort on a scale from 0 (worst) to 100 (best).
Time Frame
1-week follow up with habitual lens
Title
Subjective Comfort at End of Day With Contact Lens Wear
Description
Participants rate their end of day comfort on a scale from 0 (worst) to 100 (best).
Time Frame
Day 1 after dispense with delefilcon A
Title
Subjective Comfort at End of Day With Contact Lens Wear
Description
Participants rate their end of day comfort on a scale from 0 (worst) to 100 (best).
Time Frame
Day 3 after dispense with delefilcon A
Title
Subjective Comfort at End of Day With Contact Lens Wear
Description
Participants rate their end of day comfort on a scale from 0 (worst) to 100 (best).
Time Frame
Day 5 after dispense with delefilcon A
Title
Subjective Comfort at End of Day With Contact Lens Wear
Description
Participants rate their end of day comfort on a scale from 0 (worst) to 100 (best).
Time Frame
Day 7 after dispense with delefilcon A
Title
Subjective Comfort at End of Day With Contact Lens Wear
Description
Participants rate their end of day comfort on a scale from 0 (worst) to 100 (best).
Time Frame
Day 21 after dispense with delefilcon A
Title
Subjective Comfort at End of Day With Contact Lens Wear
Description
Participants rate their end of day comfort on a scale from 0 (worst) to 100 (best).
Time Frame
Day 28 after dispense with delefilcon A
Title
Subjective Comfort at End of Day With Contact Lens Wear
Description
Participants rate their end of day comfort on a scale from 0 (worst) to 100 (best).
Time Frame
1-month follow up with delefilcon A
Title
Subjective Rating of End of Day Dryness With Contact Lens Wear
Description
Participants rate their end of day dryness on a scale from 0 (worst) to 100 (best).
Time Frame
Day 1 after screening with habitual lenses
Title
Subjective Rating of End of Day Dryness With Contact Lens Wear
Description
Participants rate their end of day dryness on a scale from 0 (worst) to 100 (best).
Time Frame
Day 3 after screening with habitual lenses
Title
Subjective Rating of End of Day Dryness With Contact Lens Wear
Description
Participants rate their end of day dryness on a scale from 0 (worst) to 100 (best).
Time Frame
Day 5 after screening with habitual lenses
Title
Subjective Rating of End of Day Dryness With Contact Lens Wear
Description
Participants rate their end of day dryness on a scale from 0 (worst) to 100 (best).
Time Frame
1-week follow up with habitual lens
Title
Subjective Rating of End of Day Dryness With Contact Lens Wear
Description
Participants rate their end of day dryness on a scale from 0 (worst) to 100 (best).
Time Frame
Day 1 after dispense with delefilcon A
Title
Subjective Rating of End of Day Dryness With Contact Lens Wear
Description
Participants rate their end of day dryness on a scale from 0 (worst) to 100 (best).
Time Frame
Day 3 after dispense with delefilcon A
Title
Subjective Rating of End of Day Dryness With Contact Lens Wear
Description
Participants rate their end of day dryness on a scale from 0 (worst) to 100 (best).
Time Frame
Day 5 after dispense with delefilcon A
Title
Subjective Rating of End of Day Dryness With Contact Lens Wear
Description
Participants rate their end of day dryness on a scale from 0 (worst) to 100 (best).
Time Frame
Day 7 after dispense with delefilcon A
Title
Subjective Rating of End of Day Dryness With Contact Lens Wear
Description
Participants rate their end of day dryness on a scale from 0 (worst) to 100 (best).
Time Frame
Day 21 after dispense with delefilcon A
Title
Subjective Rating of End of Day Dryness With Contact Lens Wear
Description
Participants rate their end of day dryness on a scale from 0 (worst) to 100 (best).
Time Frame
Day 28 after dispense with delefilcon A
Title
Subjective Rating of End of Day Dryness With Contact Lens Wear
Description
Participants rate their end of day dryness on a scale from 0 (worst) to 100 (best).
Time Frame
1-month follow up with delefilcon A
Title
Average Lens Wear Time
Description
Average lens wear time is recorded
Time Frame
Day 1 after screening with habitual lenses
Title
Average Lens Wear Time
Description
Average lens wear time is recorded
Time Frame
Day 3 after screening with habitual lenses
Title
Average Lens Wear Time
Description
Average lens wear time is recorded
Time Frame
Day 5 after screening with habitual lenses
Title
Average Lens Wear Time
Description
Average lens wear time is recorded
Time Frame
1-week follow up with habitual lens
Title
Average Lens Wear Time
Description
Average lens wear time is recorded
Time Frame
Day 1 after dispense with delefilcon A
Title
Average Lens Wear Time
Description
Average lens wear time is recorded
Time Frame
Day 3 after dispense with delefilcon A
Title
Average Lens Wear Time
Description
Average lens wear time is recorded
Time Frame
Day 5 after dispense with delefilcon A
Title
Average Lens Wear Time
Description
Average lens wear time is recorded
Time Frame
Day 7 after dispense with delefilcon A
Title
Average Lens Wear Time
Description
Average lens wear time is recorded
Time Frame
Day 21 after dispense with delefilcon A
Title
Average Lens Wear Time
Description
Average lens wear time is recorded
Time Frame
Day 28 after dispense with delefilcon A
Title
Average Lens Wear Time
Description
Average lens wear time is recorded
Time Frame
1-month follow up with delefilcon A
Title
Comfortable Lens Wear Time
Description
Comfortable lens wear time (Time of discomfort - Time of insertion)
Time Frame
Day 1 after screening with habitual lenses
Title
Comfortable Lens Wear Time
Description
Comfortable lens wear time (Time of discomfort - Time of insertion)
Time Frame
Day 3 after screening with habitual lenses
Title
Comfortable Lens Wear Time
Description
Comfortable lens wear time (Time of discomfort - Time of insertion)
Time Frame
Day 5 after screening with habitual lenses
Title
Comfortable Lens Wear Time
Description
Comfortable lens wear time (Time of discomfort - Time of insertion)
Time Frame
1-week follow up with habitual lens
Title
Comfortable Lens Wear Time
Description
Comfortable lens wear time (Time of discomfort - Time of insertion)
Time Frame
Day 1 after dispense with delefilcon A
Title
Comfortable Lens Wear Time
Description
Comfortable lens wear time (Time of discomfort - Time of insertion)
Time Frame
Day 3 after dispense with delefilcon A
Title
Comfortable Lens Wear Time
Description
Comfortable lens wear time (Time of discomfort - Time of insertion)
Time Frame
Day 5 after dispense with delefilcon A
Title
Comfortable Lens Wear Time
Description
Comfortable lens wear time (Time of discomfort - Time of insertion)
Time Frame
Day 7 after dispense with delefilcon A
Title
Comfortable Lens Wear Time
Description
Comfortable lens wear time (Time of discomfort - Time of insertion)
Time Frame
Day 21 after dispense with delefilcon A
Title
Comfortable Lens Wear Time
Description
Comfortable lens wear time (Time of discomfort - Time of insertion)
Time Frame
Day 28 after dispense with delefilcon A
Title
Comfortable Lens Wear Time
Description
Comfortable lens wear time (Time of discomfort - Time of insertion)
Time Frame
1-month follow up with delefilcon A
10. Eligibility
Sex
All
Minimum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Is at least 17 years of age and has full legal capacity to volunteer;
Has read and signed an information consent letter;
Is willing and able to follow instructions and maintain the appointment schedule;
As per TFOS DEWS II, have dry eye symptoms (without CL wear) as determined by an OSDI score of ≥13 and at least one of the following:
Tear osmolarity ≥ 308mOsm/L or interocular difference >8 mOsm/L
Non-invasive tear breakup time of < 10 seconds in at least one eye
More than 5 spots of corneal staining OR > 9 conjunctival spots in at least one eye
Reports dryness while wearing DD CLs with CLDEQ-8 score ≥ 12 and ≤ 203
Habitually wears soft spherical DD CLs with a power between +6.00D and -10.00D
Manifest spectacle cyl ≤1.00DC in either eye
BCVA ≤0.20 log MAR each eye with habitual & DT1
Acceptable fit with habitual & DT1
Willing to wear DT1 CLs at least 3 days per week and 6 hours per day throughout the study
Exclusion Criteria:
Is participating in any concurrent clinical or research study;
Has any known active* ocular disease and/or infection;
Has a systemic condition that in the opinion of the investigator may affect a study outcome variable;
Is using any systemic or topical medications that in the opinion of the investigator may affect a study outcome variable;
Has known sensitivity to the diagnostic pharmaceuticals to be used in the study;
Is pregnant, lactating or planning a pregnancy at the time of enrolment (by self-report);
Is aphakic;
Has undergone refractive error surgery;
Has taken part in another clinical research study within the last 14 days;
Current habitual wearer of DT1
Any ocular and/or systemic conditions or concomitant medication to contraindicate contact lens wear or be expected to interfere with the primary outcome variables.
For the purposes of this study, active ocular disease is defined as infection or inflammation which requires therapeutic treatment. Mild (i.e. not considered clinically relevant) lid abnormalities (blepharitis, meibomian gland dysfunction, papillae), corneal and conjunctival staining and dry eye are not considered active ocular disease. Neovascularization and corneal scars are the result of previous hypoxia, infection or inflammation and are therefore not active.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lyndon Jones, PhD, FCOptom
Organizational Affiliation
Centre for Ocular Research & Education
Official's Role
Principal Investigator
Facility Information:
Facility Name
Centre for Ocular Research & Education
City
Waterloo
State/Province
Ontario
ZIP/Postal Code
N2B 3K4
Country
Canada
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Refitting Daily Disposable Contact Lens Wearers With Dry Eye Disease With A Different Daily Disposable Lens Type
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