Trials / Completed
CompletedNCT05097144
Performance of Toric Silicone Hydrogel Contact Lenses
Performance of Two Toric Silicone Hydrogel Contact Lenses
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 36 (actual)
- Sponsor
- CooperVision, Inc. · Industry
- Sex
- All
- Age
- 18 Years – 40 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study was to evaluate the clinical performance and subjective lens handling (insertion and removal) of two toric silicone hydrogel contact lenses after one month of daily wear each.
Detailed description
This was a prospective, randomized, double masked, bilateral, crossover study. Participants were expected to attend 6 scheduled visits over a period of approximately 2 months.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Lens A (fanfilcon A) | Daily wear for one month |
| DEVICE | Lens B (asmofilcon A) | Daily wear for one month |
Timeline
- Start date
- 2021-08-21
- Primary completion
- 2021-12-08
- Completion
- 2021-12-08
- First posted
- 2021-10-28
- Last updated
- 2023-10-17
- Results posted
- 2022-08-24
Locations
1 site across 1 country: Mexico
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT05097144. Inclusion in this directory is not an endorsement.