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

Myopia Clinical Trial

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00412568
• Other study ID #: WRAMC WU # 04-2335-99d
• Secondary ID: WU #2335-99 (mas
• Status: Completed
• Phase: N/A
• First received: December 15, 2006
• Last updated: March 31, 2008
• Start date: May 2004
• Est. completion date: March 2008

Study information

• Verified date: November 2007
• Source: Walter Reed Army Medical Center
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Federal Government
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to:

1. evaluate the safety and efficacy of conventional PRK in U.S. Army personnel who have naturally occurring myopia with or without astigmatism.

2. compare the data from this control group to study groups undergoing wavefront guided PRK.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 150
• Est. completion date: March 2008
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 21 Years and older

Eligibility

Inclusion Criteria:

1. Male or female, of any race, and at least 21 years old at the time of the pre-operative examination, and have signed an informed consent. The lower age limit of 21 years is intended to ensure documentation of refractive stability.

2. Manifest refractive spherical equivalent (MSE) of up to 6.00 diopters (D) at the spectacle plane with refractive cylinder up to 3.00 D.

3. Manifest refraction and LADARWave™ refractions must be within 1.00 D.

4. Best spectacle corrected visual acuity of 20/20 or better in both eyes.

5. Demonstrated refractive stability, confirmed by clinical records. Neither the spherical nor the cylindrical portion of the refraction may have changed more than 0.50D during the 12-month period immediately preceding the baseline examination, as confirmed by clinical records.

6. Soft contact lens users must have removed their lenses at least 2 weeks before baseline measurements. Hard contact lens users (PMMA or rigid gas permeable lenses) must have removed their lenses at least 4 weeks prior to baseline measurements and have 2 central keratometry readings and 2 manifest refractions taken at least 1 week apart that do not differ by more than 0.50 D in either meridian; mires should be regular.

7. Located in the greater Washington DC area for a 12-month period.

8. Consent of the subject's command (active duty) to participate in the study.

9. Access to transportation to meet follow-up requirements.

Exclusion Criteria:

1. Female subjects who are pregnant, breast-feeding or intend to become pregnant during the study. Female subjects will be given a urine pregnancy test prior to participating in the study to rule out pregnancy.

2. Concurrent topical or systemic medications that may impair healing, including corticosteroids, antimetabolites, isotretinoin (Accutane), amiodarone hydrochloride (Cordarone) and/or sumatripin (Imitrex).

3. Medical condition(s), which, in the judgment of the investigator, may impair healing, including but not limited to: collagen vascular disease, autoimmune disease, immunodeficiency diseases, and ocular herpes zoster or simplex.

4. Active ophthalmic disease, neovascularization of the cornea within 1mm of the intended ablation zone, or clinically significant lens opacity.

5. Evidence of glaucoma or an intraocular pressure greater than 22 mm Hg at baseline.

6. Evidence of keratoconus, corneal irregularity, or abnormal videokeratography in either eye.

7. History of recurrent erosions or epithelial basement dystrophy.

8. Patients with known sensitivity or inappropriate responsiveness to any of the medications used in the post-operative course.

9. Any physical or mental impairment that would preclude participation in any of the examinations.

Study Design

Allocation: Non-Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Myopia

Intervention

Procedure:
• Photorefractive Keratectomy (PRK)
vision correction with PRK

Locations

Country	Name	City	State
United States	Walter Reed Army Medical Center, Center For Refractive Surgery	Washington	District of Columbia

Sponsors (2)

Lead Sponsor	Collaborator
Walter Reed Army Medical Center	United States Naval Medical Center, San Diego

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	safety, efficacy, and refractive stability		one year after procedure