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
| Type | Name | Description |
|---|---|---|
| DEVICE | ProKera | ProKera placed in non-dominant eye after photorefractive keratectomy (PRK) |
| DEVICE | Bandage contact lens | Bandage 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.