Trials / Completed
CompletedNCT06098339
Performance Evaluation of Reusable Contact Lenses When Worn For One Month By Habitual Soft Contact Lens Wearers
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 53 (actual)
- Sponsor
- CooperVision, Inc. · Industry
- Sex
- All
- Age
- 18 Years – 39 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study was to compare the clinical performance of two different reusable lenses in habitual spherical soft lens wearers.
Detailed description
This study was a prospective, bilateral eye, double-masked, randomized, 1 month cross-over, daily-wear design involving two different frequent replacement type lenses. Duration of involvement for each participant was approximately 3 months.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Lens A (fanfilcon A) | Daily wear for one month |
| DEVICE | Lens B (lotrafilcon B) | Daily wear for one month |
Timeline
- Start date
- 2023-11-13
- Primary completion
- 2024-04-04
- Completion
- 2024-04-04
- First posted
- 2023-10-24
- Last updated
- 2024-08-28
- Results posted
- 2024-07-09
Locations
3 sites across 2 countries: United States, Canada
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT06098339. Inclusion in this directory is not an endorsement.