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Sponsored by: |
Walter Reed Army Medical Center |
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Information provided by: | Walter Reed Army Medical Center |
ClinicalTrials.gov Identifier: | NCT00413673 |
The objective of this study is to conduct a prospective clinical trial to evaluate the safety and efficacy fo the VISX Excimer Laser system for the treatment of naturally occurring low to moderate myopia, with or without low levels of astigmatism, in U.S. Army personnel.
Condition | Intervention |
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Myopia |
Procedure: PRK |
Study Type: | Interventional |
Study Design: | Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Safety/Efficacy Study |
Official Title: | Initial Evaluation of Photorefractive Keratectomy in U.S. Army Personnel |
Estimated Enrollment: | 100 |
Study Start Date: | August 2001 |
Estimated Study Completion Date: | March 2008 |
Arms | Assigned Interventions |
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1: Experimental
PRK
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Procedure: PRK
PRK
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Ages Eligible for Study: | 21 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
Spherical component / Maximum cylinder
Exclusion Criteria:
United States, District of Columbia | |
Walter Reed Army Medical Center, Center for Refractive Surgery | |
Washington, District of Columbia, United States, 20307 |
Principal Investigator: | KRAIG S. BOWER, MD | Walter Reed Army Medical Center |
Study ID Numbers: | WRAMC WU # 2335-99 |
Study First Received: | December 19, 2006 |
Last Updated: | March 31, 2008 |
ClinicalTrials.gov Identifier: | NCT00413673 |
Health Authority: | United States: Federal Government |
Naturally occurring low to moderate myopia, with or without low levels of astigmatism in U.S. Army personnel |
Eye Diseases Myopia Refractive Errors Astigmatism |