CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 40 enrolled
Drug / intervention
ProKera +1 moredevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00915759
NCT00915759N/ACompleted
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Sutureless Cryopreserved Amniotic Membrane Graft (ProKera) and Wound Healing After Photorefractive Keratectomy

Walter Reed National Military Medical Center·interventional·Posted Jun 8, 2009·Updated Feb 7, 2025

In Brief

A clinical study evaluating ProKera and Bandage contact lens for Corneal Wound Healing. Completed, enrolled 40 participants across 1 site.

Detailed Summary

The purpose of this study is to evaluate the effect of ProKera on corneal wound healing after photorefractive keratectomy (PRK) in terms of re-epithelialization, pain, adverse effects, visual recovery, refractive accuracy, and corneal clarity.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsCorneal Wound Healing
CountriesUnited States
CollaboratorsBioTissue Holdings, Inc, St. John's Hospital, University of Colorado, Denver

Timeline

N/ACompletedFinished
200920102011201220132014201520162017201820192020202120222023202420252026
First PostedJun 8, 2009
Enrollment StartJun 1, 2009
Primary CompletionNov 1, 2010
Study CompletionJul 1, 2015
TodayJul 2, 2026
Enrollment to primary: 1.4 yearsPosted 17.1 years ago

Interventions

ProKeradevice

ProKera placed in non-dominant eye after photorefractive keratectomy (PRK)

Bandage contact lensdevice

Bandage contact lens placed in dominant eye, the current standard after photorefractive keratectomy (PRK)