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Sponsors and Collaborators: |
Walter Reed Army Medical Center United States Naval Medical Center, San Diego |
Information provided by: | Walter Reed Army Medical Center |
ClinicalTrials.gov Identifier: | NCT00412568 |
The purpose of this study is to:
Condition | Intervention |
Myopia |
Procedure: Photorefractive Keratectomy (PRK) |
Study Type: | Interventional |
Study Design: | Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment |
Official Title: | Evaluation of Conventional Photorefractive Keratectomy (PRK) in U.S. Army Personnel, Substudy of: Initial Evaluation of Excimer Laser Keratorefractive Surgery in U.S. Army Personnel |
Estimated Enrollment: | 150 |
Study Start Date: | May 2004 |
Estimated Study Completion Date: | March 2008 |
Arms | Assigned Interventions |
1: Active Comparator
PRK control group
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Procedure: Photorefractive Keratectomy (PRK)
vision correction with PRK
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Ages Eligible for Study: | 21 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
Exclusion Criteria:
United States, District of Columbia | |||||
Walter Reed Army Medical Center, Center for Refractive Surgery | |||||
WASHINGTON, District of Columbia, United States, 20302 |
Walter Reed Army Medical Center |
United States Naval Medical Center, San Diego |
Principal Investigator: | KRAIG S. BOWER, MD | Walter Reed Army Medical Center |
Study ID Numbers: | WRAMC WU # 04-2335-99d, WU #2335-99 (master protocol) |
First Received: | December 15, 2006 |
Last Updated: | March 31, 2008 |
ClinicalTrials.gov Identifier: | NCT00412568 |
Health Authority: | United States: Federal Government |
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