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NCT00412568 · ClinicalTrials.gov registry record · NA

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

A NA study, sponsored by Walter Reed Army Medical Center.

Completed
Registry status
NA
Development phase
150
Enrollment target

NCT00412568 is a NA study that has completed, run by Walter Reed Army Medical Center. The registered enrollment target is 150 participants.

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The verdict

NCT00412568, a NA study, has completed, sponsored by Walter Reed Army Medical Center.

COMPLETED
Registry status
NA
Development phase
150 participants
Enrollment target

Study 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.

Interventions

  • PROCEDURE Photorefractive Keratectomy (PRK)

Trial Details

FieldValue
Enrollment Target 150 participants
Start Date 2004-05
Est. Completion 2008-03
Phase NA

Sponsor

Walter Reed Army Medical Center

24 total trials

What the Registry Record Tells You About NCT00412568

The ClinicalTrials.gov registry entry for NCT00412568 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 150 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Walter Reed Army Medical Center, which has 24 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Photorefractive Keratectomy (PRK) is the first listed.

NCT00412568 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00412568 about?

NCT00412568 is a clinical study titled "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". 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.

What is the current status of trial NCT00412568?

This trial is currently completed. It is a NA study. The enrollment target is 150 participants. The study started on 2004-05. Estimated completion is 2008-03.

What interventions are being tested in trial NCT00412568?

The interventions under investigation include: Photorefractive Keratectomy (PRK) (PROCEDURE).

Who is sponsoring clinical trial NCT00412568?

This trial is sponsored by Walter Reed Army Medical Center, which has 24 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.