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OpenTrials
Completed

NCT Number: NCT00713856

Comparison of Conventional and Custom Photorefractive Keratectomy (PRK)

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.

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Key information

Conditions

Myopia Eye Diseases Refractive Errors

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Utah, John Moran Eye Center

Salt Lake City, Utah, 84132, United States

About this study

Patients undergoing bilateral PRK on the same day will have one eye randomly assigned to custom wavefront guided PRK and the fellow eye treated with conventional PRK.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients deemed to be suitable candidates for bilateral PRK

Exclusion criteria

  • Patients desiring monovision correction rather than bilateral distance correction

Treatment and study plan

Custom PRK with iris registration

Procedure

PRK

Conventional PRK

Procedure

PRK

Primary outcomes

  1. Visual acuity

    Time frame: 6 months

Secondary outcomes

  1. Manifest refraction

    Time frame: 6 months

  2. Wavefront aberration value

    Time frame: 6 months

Sponsors and collaborators

Lead sponsor

University of Utah

Other

Registry information

Official study title

Comparison of Conventional and Custom With Iris Registration PRK Ablations: Assessment of Visual Function and Patient Satisfaction

Important dates

Study start
2007
Primary completion
2009
Study completion
2010
First posted
Jul 14, 2008
Registry last updated
Oct 19, 2010

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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