A Study to Evaluate the Safety and Effectiveness of the 217z Laser With Zyoptix for Lasik

Not Applicable

Withdrawn

• Conditions: Myopia; Astigmatism
• Interventions: Device: 217z Laser

• Registration Number: NCT00347997
• Lead Sponsor: Bausch & Lomb Incorporated

Brief Summary

A Study to demonstrate the safety and efficacy of wavefront laser refractive surgery treatments for myopia and astigmatism.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2006-06-30
• Study First Submitted QC: 2006-07-03
• Study First Posted: 2006-07-04
• Status Verified: 2011-12
• Last Update Submitted: 2011-12-07
• Last Update Posted: 2011-12-08

Recruitment & Eligibility

• Status: WITHDRAWN
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

• Myopia with or without astigmatism.

Exclusion Criteria

• Contraindications to LASIK.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
LASIK	217z Laser	LASIK correction of myopia and myopic astigmatism

Primary Outcome Measures

Name	Time	Method
Visual acuity	24 months