A Study to Evaluate the Safety and Effectiveness of the Technols 217z Zyoptix System for Hyperopia

Bausch + Lomb

Status: Completed

Conditions: Astigmatism; Hyperopia

Treatments: Device: Technolas 217z Zyoptix Laser

Study type: Interventional

Funder types: Industry

Identifiers

NCT00348205

369

Details and patient eligibility

About

A study to demonstrate the safety and effectiveness of wavefront laser refractive surgery treatments for hyperopia and astigmatism.

Enrollment: 80 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Hyperopia with or without astigmatism.

Exclusion criteria

• Contraindications to LASIK.

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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80 participants in 1 patient group

Technolas 217z Zyoptix System

Experimental group

Description:

Bausch \& Lomb Technolas 217z Zyoptix System with Treatment Planner Customized Treatment Calculation Software.

Treatment:

Device: Technolas 217z Zyoptix Laser