Trials / Completed
CompletedNCT05933772
Performance Evaluation of Two Silicone Hydrogel Toric Lens Designs in Habitual Soft Contact Lens Wearers
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 50 (actual)
- Sponsor
- CooperVision International Limited (CVIL) · Industry
- Sex
- All
- Age
- 18 Years – 39 Years
- Healthy volunteers
- Accepted
Summary
The objective of the study was to compare the clinical performance of two monthly toric silicone hydrogel contact lenses in habitual wearers, when worn for 1-month each.
Detailed description
This study was a prospective, bilateral eye, subjected-masked, randomized, 1-month cross-over, daily-wear design involving two different silicone hydrogel toric lens types. Each lens type will be worn bilaterally for approximately one month.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Lens A (comfilcon A toric lens) | One month wear |
| DEVICE | Lens B (lehfilcon A toric lens) | One month wear |
Timeline
- Start date
- 2023-08-18
- Primary completion
- 2023-12-28
- Completion
- 2023-12-28
- First posted
- 2023-07-06
- Last updated
- 2025-03-11
- Results posted
- 2025-03-10
Locations
5 sites across 2 countries: United States, Canada
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT05933772. Inclusion in this directory is not an endorsement.