Clinical Trials Directory

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

TypeNameDescription
DEVICESupracorThe 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.