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COMPLETEDPhase 4NCT03123614

Loteprednol vs. Prednisolone and Fluorometholone

Corneal haze, in which the cornea becomes cloudy, is a well-known and a potentially vision-threatening postoperative complication of photorefractive keratectomy (PRK). Topical ophthalmic corticosteroi...

Lead sponsor: University of Utah•1 U.S. locations•View source on ClinicalTrials.gov

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Sponsors

Lead Sponsor

University of Utah

Age

21 - No limit years

Sex

ALL

Healthy Volunteers

No

Inclusion Criteria

•All subjects who are deemed suitable candidates for PRK after routine refractive surgery screening will be considered eligible for participation in this study.
•Subjects must be at least 21 years of age and not pregnant or nursing (due to fluctuations in visual parameters during pregnancy).

Exclusion Criteria

•Selection will be consistent with the current standard of care for PRK. Any patient that is not a suitable candidate for PRK will not be included.

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: May 26, 2021Terms

Trial snapshot

StatusCOMPLETED

PhasePHASE4

Enrollment131

Start dateSep 2014

Last updatedMay 26, 2021

Condition

Intraocular Pressure Corneal Opacity

Locations shown

Moran Eye Center - Midvalley Location

Murray, Utah

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: May 26, 2021Data synced to Clareo: June 28, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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