Trials / Completed
CompletedNCT00838045
Evaluation of the Safety & Effectiveness of the Bausch & Lomb AKREOS® TL Intraocular Lens
A Prospective, Multi-Center Clinical Investigation to Evaluate the Safety & Effectiveness of the Bausch & Lomb AKREOS® TL (Model MI60) Intraocular Lens
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 125 (actual)
- Sponsor
- Bausch & Lomb Incorporated · Industry
- Sex
- All
- Age
- 50 Years – 79 Years
- Healthy volunteers
- Not accepted
Summary
This study is to evaluate the safety and effectiveness of the Bausch \& Lomb Akreos TL (thin lens) intraocular lens (IOL) following implantation in adults requiring cataract surgery.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | The Bausch & Lomb Akreos TL IOL (MI60) posterior chamber IOL | Surgery to implant the Bausch \& Lomb Akreos TL Intraocular Lens will be performed using standard microsurgical techniques following cataract surgery. |
Timeline
- Start date
- 2006-09-01
- Primary completion
- 2008-04-01
- Completion
- 2008-09-01
- First posted
- 2009-02-06
- Last updated
- 2011-12-09
Locations
1 site across 1 country: Germany
Source: ClinicalTrials.gov record NCT00838045. Inclusion in this directory is not an endorsement.