Trials / Completed
CompletedNCT01100411
Changes in Invitro and ex Vivo Lens Metrology With Daily Wear Contact Lenses
Changes in Invitro and ex Vivo Lens Metrology With Experienced Daily Wear Contact Lens Wearers
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 35 (actual)
- Sponsor
- Alcon Research · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Accepted
Summary
The purpose of this study is to evaluate changes in contact lens geometry after lens wear
Detailed description
The purpose of this study is to evaluate changes invitro and ex vivo in contact lens geometry in daily lens wear
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Air Optix Aqua | Contact lens material: Lotrafilcon A |
| DEVICE | Biofinity | Contact lens material: Comfilcon A |
| DEVICE | Proclear | Contact lens material: Omafilcon A |
| DEVICE | Acuvue Oasys | Contact lens material: Senofilcon A |
| DEVICE | Acuvue 2 | Contact lens material: Etafilcon A |
| DEVICE | Purevision | Contact lens material: Balafilcon A |
Timeline
- Start date
- 2010-03-01
- Primary completion
- 2010-07-01
- Completion
- 2010-07-01
- First posted
- 2010-04-09
- Last updated
- 2012-07-18
Locations
1 site across 1 country: Australia
Source: ClinicalTrials.gov record NCT01100411. Inclusion in this directory is not an endorsement.