Trials / Unknown
UnknownNCT02071576
A Prospective Safety and Effectiveness Study of the 500 Hz Technolas Perfect Vision Excimer Laser Using LASIK
- Status
- Unknown
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 42 (estimated)
- Sponsor
- Technolas Perfect Vision GmbH · Industry
- Sex
- All
- Age
- 18 Years – 85 Years
- Healthy volunteers
- Not accepted
Summary
This clinical study has been planned to evaluate the safety and effectiveness of a common treatment algorithms (Proscan) using 500 Hz laser repetition rate.
Detailed description
This clinical study has been planned to evaluate the safety and effectiveness of the excimer laser treatment algorithm Proscan of the 500 Hz laser system for ametropia when performed on the cornea of virgin eyes.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Proscan | One device (500 Hz Excimer Laser - TENEO) with one intervention (Proscan) |
Timeline
- Start date
- 2014-02-01
- Primary completion
- 2015-08-01
- Completion
- 2016-08-01
- First posted
- 2014-02-26
- Last updated
- 2014-11-20
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT02071576. Inclusion in this directory is not an endorsement.