Trials / Completed
CompletedNCT03226353
Performance of Somofilcon A Over One Week in Wearers Adapted to Omafilcon A
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 77 (actual)
- Sponsor
- CooperVision, Inc. · Industry
- Sex
- All
- Age
- 17 Years
- Healthy volunteers
- Accepted
Summary
The objective of the study is to determine if habitual or adapted contact lens wearers of Omafilcon A can be confidently refit into Somofilcon A lenses and be successful after one week of daily wear. The primary outcome variables for this study are: * Investigator responses to refit questions; * Lens fit.
Detailed description
This is a prospective, single-site, dispensing, bilateral wear, open label, daily wear switch study, with the test lens (Somofilcon A) being worn for 7 (+5) days.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | somofilcon A | contact lens |
| DEVICE | omafilcon A | contact lens |
Timeline
- Start date
- 2017-07-06
- Primary completion
- 2017-09-27
- Completion
- 2017-09-27
- First posted
- 2017-07-21
- Last updated
- 2019-09-12
- Results posted
- 2019-02-04
Locations
1 site across 1 country: Canada
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT03226353. Inclusion in this directory is not an endorsement.