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Comparison of Conventional and Custom Photorefractive Keratectomy (PRK)

NCT00713856 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 44

Last updated 2010-10-19

No results posted yet for this study

Summary

The study objective is to compare the clinical outcomes using wavefront guided PRK with iris registration and conventional laser PRK using FDA-approved laser technology on the same patient.

Conditions

  • Myopia

Interventions

PROCEDURE

Custom PRK with iris registration

PRK

PROCEDURE

Conventional PRK

PRK

Sponsors & Collaborators

Principal Investigators

  • Mark Mifflin, MD · University of Utah

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-11-30
Primary Completion
2009-12-31
Completion
2010-05-31

Countries

  • United States

Study Locations

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Entities

Companies

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 NCT00713856 on ClinicalTrials.gov