Trials / Completed
CompletedNCT02450799
Corrected VA With Long-Term Follow-Up After AcrySof® Intraocular Lens (IOL) Implantation
Corrected VA With Long-Term Follow-Up After AcrySof® IOL Implantation
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 104 (actual)
- Sponsor
- Alcon, a Novartis Company · Industry
- Sex
- All
- Age
- —
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to compare the long-term visual acuity (VA) with an acrylic IOL to a silicone or polymethylmethacrylate (PMMA) IOL in cataract patients. This study will take place in Japan.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Acrylic IOL | Acrylic IOL for long-term implantation in the cataract patient |
| DEVICE | Silicone IOL | Silicone IOL for long-term implantation in the cataract patient |
| DEVICE | PMMA IOL | Polymethylmethacrylate IOL for long-term implantation in the cataract patient |
Timeline
- Start date
- 2015-06-01
- Primary completion
- 2016-05-01
- Completion
- 2016-05-01
- First posted
- 2015-05-21
- Last updated
- 2016-12-09
- Results posted
- 2016-12-09
Source: ClinicalTrials.gov record NCT02450799. Inclusion in this directory is not an endorsement.