Trials / Completed
CompletedNCT02965820
OPTI-FREE® PureMoist® for Presbyopic Contact Lens Wearers
Clinical Study of OPTI-FREE® PureMoist® for Presbyopic Contact Lens Wearers
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 122 (actual)
- Sponsor
- Alcon, a Novartis Company · Industry
- Sex
- All
- Age
- 45 Years – 65 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to evaluate OPTI-FREE® PureMoist® (OFPM) compared to non-HYDRAGLYDE® multi-purpose contact lens solutions in presbyopes currently wearing soft contact lenses and experiencing symptoms of dryness.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Opti-Free® PureMoist® contact lens solution | |
| DEVICE | Habitual Multi-Purpose Contact Lens Solution | |
| DEVICE | Habitual Contact Lenses | Subject's habitual contact lens brand worn in a daily wear modality for 30 days. |
Timeline
- Start date
- 2016-12-16
- Primary completion
- 2017-04-01
- Completion
- 2017-04-01
- First posted
- 2016-11-17
- Last updated
- 2018-07-12
- Results posted
- 2018-04-26
Source: ClinicalTrials.gov record NCT02965820. Inclusion in this directory is not an endorsement.