Trials / Completed
CompletedNCT02588573
Overall Performance of a 1-day Silicone Hydrogel Lens When Habitual Soft Lens Wearers Are Refit
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 103 (actual)
- Sponsor
- CooperVision, Inc. · Industry
- Sex
- All
- Age
- 17 Years
- Healthy volunteers
- Accepted
Summary
The objective of the study is to compare the overall subjective comfort profile over 8 hours of lens wear in two groups of habitual soft contact lens wearers (daily disposable hydrogel lenses and frequent replacement lenses) when refitted in to somofilcon A lenses.
Detailed description
This will be a prospective, single day, randomized, double-masked, non-dispensing, contralateral study. Participants were recruited into one of two groups - participants who habitually wore etafilcon A: daily disposable hydrogel lenses and participants who habitually wore frequent replacement lenses (FREQ).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | etafilcon A (control) | contact lens |
| DEVICE | somofilcon A (test) | contact lens |
Timeline
- Start date
- 2015-10-01
- Primary completion
- 2016-03-01
- Completion
- 2016-04-01
- First posted
- 2015-10-28
- Last updated
- 2019-02-08
- Results posted
- 2019-02-08
Locations
2 sites across 1 country: Canada
Source: ClinicalTrials.gov record NCT02588573. Inclusion in this directory is not an endorsement.