Trials / Completed
CompletedNCT03306641
A One-Week Crossover Dispensing Evaluation of New Daily Wear Soft Contact Lenses
A One-Week Crossover Dispensing Evaluation of Gemini Daily Wear Soft Contact Lenses
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 45 (actual)
- Sponsor
- CooperVision, Inc. · Industry
- Sex
- All
- Age
- 18 Years – 55 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to validate the clinical performance of a new contact lens design when worn over a period 1 week compared to nelfilcon A (control).
Detailed description
The purpose of this study is to validate the clinical performance of a new contact lens design when worn over a period of 1 week compared to nelfilcon A (control). The primary outcomes of interest is lens fit acceptance.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Test Contact Lens | Daily disposable contact lens |
| DEVICE | Nelfilcon A | Focus Dailies All Day Comfort contact lens (nelfilcon A) |
Timeline
- Start date
- 2017-07-28
- Primary completion
- 2017-08-31
- Completion
- 2017-08-31
- First posted
- 2017-10-11
- Last updated
- 2020-09-22
- Results posted
- 2020-09-22
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT03306641. Inclusion in this directory is not an endorsement.