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

Bausch + Lomb

Status: Withdrawn

Conditions: Myopia; Astigmatism

Treatments: Device: 217z Laser

Study type: Interventional

Funder types: Industry

Identifiers

NCT00347997

385

Details and patient eligibility

About

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

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Myopia with or without astigmatism.

Exclusion criteria

• Contraindications to LASIK.

Trial design

Primary purpose: Treatment

Allocation: Non-Randomized

Interventional model: Single Group Assignment

Masking: None (Open label)

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0 participants in 1 patient group

LASIK

Experimental group

Description:

LASIK correction of myopia and myopic astigmatism

Treatment:

Device: 217z Laser