Trials / Completed
CompletedNCT01225952
Three Intraocular Lenses Designed to Improve Distance, Intermediate and Near Vision Following Lens Extraction
A Three Arm Prospective Clinical Evaluation of Three FDA-approved Intraocular Lenses Designed to Improve Distance, Intermediate and Near Vision Following Lens Extraction
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 93 (actual)
- Sponsor
- Bausch & Lomb Incorporated · Industry
- Sex
- All
- Age
- 40 Years
- Healthy volunteers
- Not accepted
Summary
The objective of this study is to compare the contrast sensitivity, high and low contrast visual acuity (VA), glare meter outcomes, and subject satisfaction with three different FDA-approved intraocular lenses (IOLs) designed to improve distance, intermediate, and near vision following lens extraction in adults at least 40 years of age.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Crystalens AO | Bausch \& Lomb model silicone multi-piece accommodating IOL. |
| DEVICE | ReSTOR 3.0 | An aspheric multifocal IOL (Alcon Laboratories) combines the functions of an apodized diffractive region and a refractive region. |
| DEVICE | AMO Tecnis Multifocal | The Tecnis Multifocal foldable hydrophobic acrylic IOL, Model ZMA00 (Abbott Medical Optics), is an ultraviolet light-absorbing posterior chamber IOL. |
Timeline
- Start date
- 2010-07-01
- Primary completion
- 2011-06-01
- Completion
- 2011-07-01
- First posted
- 2010-10-21
- Last updated
- 2013-01-18
- Results posted
- 2013-01-18
Locations
1 site across 1 country: Philippines
Source: ClinicalTrials.gov record NCT01225952. Inclusion in this directory is not an endorsement.