Wavefront-guided Photorefractive Keratectomy (PRK) Versus Wavefront-guided Lasik for Myopia

Not Applicable

Completed

• Conditions: Myopia; Astigmatism
• Interventions: Procedure: Photorefractive keratectomy; Procedure: Laser in-situ keratomileusis

• Registration Number: NCT01140594
• Lead Sponsor: Stanford University

Brief Summary

A prospective comparison of eyes undergoing wavefront-guided LASIK in one eye and wavefront-guided PRK in their fellow eye for myopia.

Detailed Description

This is a research study comparing the outcomes of LASIK surgery to PRK surgery for nearsightedness when using the two different procedures. You will have one eye treated with LASIK using the Intralase FS laser and your other eye treated with PRK. You will be one of 100 sighted patients at Stanford to undergo treatment in this clinical research trial. This will be a prospective, randomized, research study in which up to 200 consecutive eyes scheduled to undergo excimer laser in situ keratomileusis (LASIK) in one eye and photorefractive keratectomy (PRK) in the fellow eye for the correction of myopia (nearsightedness) with or without astigmatism will be enrolled. The choice of which eye receives LASIK and which eye receives PRK will be randomized prior to enrollment. Randomization will be done according to a randomization schedule. You will know which eye is being treated with which procedure. The randomization will determine only whether your right or left eye is treated with the LASIK procedure. The other eye will be treated with PRK. You have a fifty percent chance of having your left eye treated with LASIK as your right eye. Subjects will undergo either bilateral (both eyes at once) wavefront (a more precise custom laser system) guided LASIK and PRK treatments using the VISX Star S4 excimer laser. All subjects will be followed for one year after the vision correction procedure. Subjects scheduled to undergo LASIK and PRK for the correction of myopia (nearsightedness) with or without astigmatism will be screened for eligibility. Eligible subjects will be examined preoperatively to establish a baseline for ocular condition (the general health and glasses prescription of the eyes). Postoperatively, subjects will undergo an ophthalmic evaluation (complete eye examination) at regular intervals as specified in this protocol. Retreatments (a second operation on the same eye for residual nearsightedness) will not be allowed during the first six months of this study. If you elect to undergo a retreatment of your LASIK or PRK surgery prior to the 6-month post-operative visit, the retreated eye will be exited from the study as of the retreatment date.

Any significant new finding developed during the course of the research which may relate to the subject's willingness to continue participation will be provided to the subject or subject's representative in a timely manner.

Basic Information
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Recruitment & Eligibility
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Study & Design
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Trial Locations

Study Timeline

• Study Start: 2006-08
• Primary Completion: 2008-01
• Study Completion: 2008-01
• Study First Submitted: 2010-06-02
• Study First Submitted QC: 2010-06-08
• Study First Posted: 2010-06-09
• Status Verified: 2022-04
• Last Update Submitted: 2022-04-03
• Last Update Posted: 2022-04-11

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 34

Inclusion Criteria

• Subjects age 21 and older with healthy eyes.
• Nearsightedness between -0.75 diopters and -7.00 diopters with or without astigmatism of up to -3.50 diopters.

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Exclusion Criteria

• Subjects under the age of 21.
• Patients with thin corneas.
• Patients with topographic irregularities.
• Patients with keratoconus.
• Patients with autoimmune diseases.
• Patients who are pregnant or nursing.
• Patients must have similar levels of nearsightedness in each eye. They can not be more than 1.0 diopter of difference between eyes.
• Patients must have similar levels of astigmatism in each eye. They can not have more than 1.0 diopter of difference between eyes.

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Wavefront-guided LASIK	Laser in-situ keratomileusis	Wavefront-guided LASIK
Wavefront-guided PRK	Laser in-situ keratomileusis	Wavefront-guided PRK
Wavefront-guided LASIK	Photorefractive keratectomy	Wavefront-guided LASIK
Wavefront-guided PRK	Photorefractive keratectomy	Wavefront-guided PRK

Primary Outcome Measures

Name	Time	Method
Changes in 25 and 5% low contrast acuity	baseline to one year
Changes in best spectacle corrected visual acuity	Baseline to one year
Improvement in uncorrected visual acuity	Baseline to one year

Secondary Outcome Measures

Name	Time	Method
Changes in higher order aberrations	Baseline to one year
Comparison of dry eye signs and symptoms between LASIK and PRK	baseline to one year
Changes in quality of vision	baseline to one year

Trial Locations

Locations (1)

Stanford University School of Medicine; 🇺🇸 Stanford, California, United States