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

NCT00347997 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2011-12-08

No results posted yet for this study

Summary

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

Conditions

  • Myopia
  • Astigmatism

Interventions

DEVICE

217z Laser

LASIK correction of myopia and myopic astigmatism

Sponsors & Collaborators

  • Bausch & Lomb Incorporated

    lead INDUSTRY

Principal Investigators

  • Mohinder Merchea, OD, PhD · Bausch & Lomb Incorporated

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00347997 on ClinicalTrials.gov