Trials / Completed
CompletedNCT00449267
Aurolab Hydrophobic Foldable Intraocular Lens Study
Clinical Evaluation of Hydrophobic Foldable Intraocular Lenses
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 120 (actual)
- Sponsor
- Aurolab · Academic / Other
- Sex
- All
- Age
- 40 Years – 65 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to evaluate whether hydrophobic intraocular lenses manufactured by aurolab are safe and effective in the surgical treatment of cataract.
Detailed description
Hydrophobic as the name suggests is fear for water. Hydrophobic foldable IOLs are made from acrylic material. Aurolab has developed its own hydrophobic acrylic material. This material has been subjected to several biocompatibility studies and it has proved itself to be biocompatible.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Intraocular Lens | Phacoemulsification with in the bag implantation of the IOL |
Timeline
- Start date
- 2007-03-01
- Primary completion
- 2007-12-01
- Completion
- 2007-12-01
- First posted
- 2007-03-20
- Last updated
- 2009-02-11
Locations
1 site across 1 country: India
Source: ClinicalTrials.gov record NCT00449267. Inclusion in this directory is not an endorsement.