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NCT00414011 · ClinicalTrials.gov registry record · NA

Comparison of the Effect of 4th Generation Fluoroquinolones, Gatifloxacin and Moxifloxacin, on Epithelial Healing Following Photorefractive Keratectomy (PRK), A Substudy of: Initial Evaluation of Excimer Laser Keratorefractive Surgery in U.S. Army Personnel (WU # 2335-99)

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

Completed
Registry status
NA
Development phase
40
Enrollment target

NCT00414011: Completed NA study, sponsored by Walter Reed Army Medical Center.

NCT00414011 is a NA study that has completed, run by Walter Reed Army Medical Center. The registered enrollment target is 40 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00414011, a NA study, has completed, sponsored by Walter Reed Army Medical Center.

COMPLETED
Registry status
NA
Development phase
40 participants
Enrollment target

Study Summary

The purpose of this study is a prospective,double-blinded, randomized trial to compare the rate of healing following PRK after the use of two commercially available 4th generation fluoroquinolones, moxifloxacin and gatifloxacin.

Primary Outcome

patients' eyes will be observed daily after surgery until the corneal epithelium has completely healed (usually 3 to 4 days)

Interventions

  • DRUG Moxifloxacin
  • DRUG Gatifloxacin

Trial Details

FieldValue
Enrollment Target 40 participants
Est. Completion 2005-02
Phase NA
Walter Reed Army Medical Center

24 total trials

What the finished NCT00414011 record still lists

NCT00414011 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower).

The record links to 0 conditions, and to 2 interventions - of which Moxifloxacin is the first listed.

NCT00414011 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00414011 about?

NCT00414011 is a clinical study titled "Comparison of the Effect of 4th Generation Fluoroquinolones, Gatifloxacin and Moxifloxacin, on Epithelial Healing Following Photorefractive Keratectomy (PRK), A Substudy of: Initial Evaluation of Excimer Laser Keratorefractive Surgery in U.S. Army Personnel (WU # 2335-99)". The purpose of this study is a prospective,double-blinded, randomized trial to compare the rate of healing following PRK after the use of two commercially available 4th generation fluoroquinolones, moxifloxacin and gatifloxacin.

What is the current status of trial NCT00414011?

This trial is currently completed. It is a NA study. The enrollment target is 40 participants. Estimated completion is 2005-02.

What interventions are being tested in trial NCT00414011?

The interventions under investigation include: Moxifloxacin (DRUG), Gatifloxacin (DRUG).

Who is sponsoring clinical trial NCT00414011?

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

How this trial's enrollment target compares

Where NCT00414011's enrollment target sits among peer trials

40 1447th of 2000 higher than 465 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00414011, the US trial registry maintained by the National Library of Medicine. NCT00414011 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.