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NCT00413881 · ClinicalTrials.gov registry record · NA
A Prospective Comparison of Alcon LADARVision Wavefront-guided LASIK Enhancement and Conventional LASIK Enhancement for the Correction of Residual Refractive Errors Following LASIK Procedures
A NA study, sponsored by Walter Reed Army Medical Center.
- Completed
- Registry status
- NA
- Development phase
- 50
- Enrollment target
NCT00413881 is a NA study that has completed, run by Walter Reed Army Medical Center. The registered enrollment target is 50 participants.
The verdict
NCT00413881, a NA study, has completed, sponsored by Walter Reed Army Medical Center.
- COMPLETED
- Registry status
- NA
- Development phase
- 50 participants
- Enrollment target
Study Summary
The purpose of this study is to conduct a prospective clinical trial to compare conventional and WFG LASIK for enhancements on post-LASIK patients. Differences in safety, efficacy, visual quality, and refractive stability will also be compared during this study.
Interventions
- PROCEDURE WAVEFRONT- GUIDED LASIK ENHANCEMENT
- PROCEDURE CONVENTIONAL LASIK ENHANCEMENT
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2004-07 |
| Est. Completion | 2008-03 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00413881
The ClinicalTrials.gov registry entry for NCT00413881 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 50 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 2 interventions - of which WAVEFRONT- GUIDED LASIK ENHANCEMENT is the first listed.
NCT00413881 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00413881 about?
NCT00413881 is a clinical study titled "A Prospective Comparison of Alcon LADARVision Wavefront-guided LASIK Enhancement and Conventional LASIK Enhancement for the Correction of Residual Refractive Errors Following LASIK Procedures". The purpose of this study is to conduct a prospective clinical trial to compare conventional and WFG LASIK for enhancements on post-LASIK patients. Differences in safety, efficacy, visual quality, and refractive stability will also be compared during this study.
What is the current status of trial NCT00413881?
This trial is currently completed. It is a NA study. The enrollment target is 50 participants. The study started on 2004-07. Estimated completion is 2008-03.
What interventions are being tested in trial NCT00413881?
The interventions under investigation include: WAVEFRONT- GUIDED LASIK ENHANCEMENT (PROCEDURE), CONVENTIONAL LASIK ENHANCEMENT (PROCEDURE).
Who is sponsoring clinical trial NCT00413881?
This trial is sponsored by Walter Reed Army Medical Center, which has 24 total clinical trials registered on ClinicalTrials.gov.
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