Trials / Completed
CompletedNCT01684046
Evaluation of the Effectiveness of Two Marketed Multi-Purpose Solutions for Silicone Hydrogel Contact Lenses - Study 2
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 196 (actual)
- Sponsor
- Alcon Research · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study was to evaluate the performance of Opti-Free® PureMoist® Multi-purpose Disinfecting Solution (MPDS) compared to AMO RevitaLens OcuTec® MPDS (US brand name)/COMPLETE RevitaLens (Europe brand name) in silicone hydrogel contact lens wearers.
Detailed description
In this 2-period crossover study, eligible participants were randomized to either Opti-Free® PureMoist MPDS or RevitaLens MPDS in Period 1 for use with their habitual contact lenses, after which they switched to the alternate solution in Period 2. Each period was 30 days in length. A 2-day washout period during which participants refrained from using a multi-purpose contact lens solution preceded Period 1 and Period 2.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Opti-Free® PureMoist® MPDS | |
| DEVICE | RevitaLens MPDS | |
| DEVICE | Habitual Contact Lenses | Silicone hydrogel contact lenses per participant's habitual brand, prescription, and replacement schedule worn on a daily wear basis for at least 8 hours a day, 5 days a week for the duration of the study. During the washout period, the contact lenses were worn on a daily disposable basis. |
Timeline
- Start date
- 2012-11-01
- Primary completion
- 2013-03-01
- Completion
- 2013-03-01
- First posted
- 2012-09-12
- Last updated
- 2014-04-29
- Results posted
- 2014-04-29
Source: ClinicalTrials.gov record NCT01684046. Inclusion in this directory is not an endorsement.