Clinical Trials Directory

Trials / Completed

CompletedNCT00915759

Sutureless Cryopreserved Amniotic Membrane Graft (ProKera) and Wound Healing After Photorefractive Keratectomy

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
40 (actual)
Sponsor
Walter Reed National Military Medical Center · Federal
Sex
All
Age
21 Years – 65 Years
Healthy volunteers
Accepted

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.

Conditions

Interventions

TypeNameDescription
DEVICEProKeraProKera placed in non-dominant eye after photorefractive keratectomy (PRK)
DEVICEBandage contact lensBandage contact lens placed in dominant eye, the current standard after photorefractive keratectomy (PRK)

Timeline

Start date
2009-06-01
Primary completion
2010-11-01
Completion
2015-07-01
First posted
2009-06-08
Last updated
2025-02-07
Results posted
2013-09-20

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00915759. Inclusion in this directory is not an endorsement.

Sutureless Cryopreserved Amniotic Membrane Graft (ProKera) and Wound Healing After Photorefractive Keratectomy (NCT00915759) · Clinical Trials Directory