Trials / Completed
CompletedNCT02642991
Dispensing Study for a New Study Lens
Dispensing Study for The Phenacite Project
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 44 (actual)
- Sponsor
- CooperVision, Inc. · Industry
- Sex
- All
- Age
- 18 Years – 35 Years
- Healthy volunteers
- Not accepted
Summary
This study investigated the performance criteria over one week of daily wear to determine if the comfilcon A asphere lens (test) performed equivalently to the comfilcon A sphere (control) in terms of measurement and subjective ratings of visual performance.
Detailed description
This study was a prospective, single site, daily wear, double masked, randomized bilateral cross over dispensing study of binocular wear of comfilcon A asphere lens (test) and comfilcon A sphere lens (control) over 1 week of daily wear.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Phenacite | contact lens |
| DEVICE | comfilcon A | contact lens |
Timeline
- Start date
- 2015-11-01
- Primary completion
- 2016-01-01
- Completion
- 2016-03-01
- First posted
- 2015-12-30
- Last updated
- 2020-12-01
- Results posted
- 2020-12-01
Locations
3 sites across 2 countries: United States, Canada
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT02642991. Inclusion in this directory is not an endorsement.