Trials / Completed
CompletedNCT01496066
Calhoun Vision Light Adjustable Lens (LAL) in Subjects With Pre-Existing Corneal Astigmatism
A Prospective Randomized Controlled Multi-Center Clinical Study to Evaluate the Safety and Effectiveness of the Light Adjustable Lens (LAL) in Subjects With Pre-Existing Corneal Astigmatism
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 600 (actual)
- Sponsor
- Calhoun Vision, Inc. · Industry
- Sex
- All
- Age
- 40 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
The purpose is to evaluate the Calhoun Vision Light Adjustable Lens (LAL) and Light Delivery Device (LDD) for reducing astigmatism and improving uncorrected vision after implantation.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | LAL (Light Adjustable Lens) and Light Deliver Device (LDD) | LAL implanted and adjusted with LDD |
| DEVICE | Monofocal control IOL | Commercially available monofocal intraocular lens (IOL) |
Timeline
- Start date
- 2011-12-01
- Primary completion
- 2016-06-01
- Completion
- 2016-06-01
- First posted
- 2011-12-21
- Last updated
- 2018-06-29
- Results posted
- 2018-03-05
Locations
17 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT01496066. Inclusion in this directory is not an endorsement.