Trials / Terminated
TerminatedNCT00804726
Evaluation of the Safety and Effectiveness of the Akreos MI Five-0 Intraocular Lens.
A Prospective, Open-label, Monocular Feasibility Clinical Evaluation of the Bausch & Lomb Akreos MI Five-O Accommodating Intraocular Lens.
- Status
- Terminated
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 10 (actual)
- Sponsor
- Bausch & Lomb Incorporated · Industry
- Sex
- All
- Age
- 50 Years
- Healthy volunteers
- Not accepted
Summary
The objective of this 12-month clinical investigation is to evaluate the safety and effectiveness of the Bausch \& Lomb Akreos MI Five-O intraocular lens (IOL). Effectiveness will be shown through the demonstration of accurate distance correction and safety will be demonstrated through the monitoring of adverse events.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Akreos MI Five-O | Small incision cataract surgery with phacoemulsification cataract extraction and Akreos MI Five-O IOL surgical implantation |
Timeline
- Start date
- 2008-11-01
- Primary completion
- 2010-05-01
- Completion
- 2010-07-01
- First posted
- 2008-12-09
- Last updated
- 2014-01-17
Locations
1 site across 1 country: Germany
Source: ClinicalTrials.gov record NCT00804726. Inclusion in this directory is not an endorsement.