Trials / Completed
CompletedNCT01387360
Presbyopic Supracor Treatment for Near Myopic/Hyperopic Pseudophakic Eyes
A Prospective Study to Evaluate the Safety and Effectiveness of the Supracor Presbyopic Treatment Algorithm for Pseudophakic Eyes Using Lasik
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 33 (actual)
- Sponsor
- Technolas Perfect Vision GmbH · Industry
- Sex
- All
- Age
- 45 Years – 85 Years
- Healthy volunteers
- Not accepted
Summary
This clinical study has been planned to determine the effectiveness of a special laser treatment intended to correct both near and distance vision in patients who have undergone previous cataract surgery.
Detailed description
This clinical study has been planned to evaluate the safety and effectiveness of the SUPRACOR presbyopic excimer laser treatment algorithm for near myopic and near hyperopic indications, with or without astigmatism, when performed on the cornea of pseudophakic eyes implanted with a monofocal IOL.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Supracor | The presbyopic treatment consists of a standard treatment for distance vision and the procedure known as SUPRACOR addition to correct near vision. The SUPRACOR addition provides a multifocal ablation with a central near addition with an aberration controlled transition zone towards the periphery, thereby allowing good focus over a range of object distances. |
Timeline
- Start date
- 2011-06-01
- Primary completion
- 2013-10-01
- Completion
- 2014-10-01
- First posted
- 2011-07-04
- Last updated
- 2015-05-20
Locations
1 site across 1 country: Philippines
Source: ClinicalTrials.gov record NCT01387360. Inclusion in this directory is not an endorsement.