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NCT00713856 · ClinicalTrials.gov registry record · NA
Comparison of Conventional and Custom Photorefractive Keratectomy (PRK)
A NA study of Myopia, sponsored by University of Utah.
- Completed
- Registry status
- NA
- Development phase
- 44
- Enrollment target
- 1
- Study location
NCT00713856: Completed NA study of Myopia, sponsored by University of Utah.
NCT00713856 is a NA study of Myopia that has completed, run by University of Utah. The registered enrollment target is 44 participants, below the 267-participant average among 90 other Myopia trials with a reported enrollment target (84% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00713856, a NA study of Myopia, has completed, sponsored by University of Utah.
- COMPLETED
- Registry status
- NA
- Development phase
- 44 participants
- Enrollment target
- 1
- Study location
Study Summary
The study objective is to compare the clinical outcomes using wavefront guided PRK with iris registration and conventional laser PRK using FDA-approved laser technology on the same patient.
Conditions Studied
Interventions
- PROCEDURE Custom PRK with iris registration
- PROCEDURE Conventional PRK
Study Locations (1)
Utah
- University of Utah, John Moran Eye Center - Salt Lake City
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 44 participants |
| Start Date | 2007-11 |
| Est. Completion | 2010-05 |
| Phase | NA |
What the finished NCT00713856 record still lists
NCT00713856 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 44 participants, a relatively small participant target, below the 267-participant average among 90 other Myopia trials with a reported enrollment target (84% lower).
The record links to 1 condition, with Myopia appearing as the primary indexed condition, and to 2 interventions - of which Custom PRK with iris registration is the first listed.
NCT00713856 reports a single indexed study location in Utah.
Frequently Asked Questions
What is clinical trial NCT00713856 about?
NCT00713856 is a clinical study titled "Comparison of Conventional and Custom Photorefractive Keratectomy (PRK)". The study objective is to compare the clinical outcomes using wavefront guided PRK with iris registration and conventional laser PRK using FDA-approved laser technology on the same patient.
What is the current status of trial NCT00713856?
This trial is currently completed. It is a NA study. The enrollment target is 44 participants. The study started on 2007-11. Estimated completion is 2010-05.
What conditions does trial NCT00713856 study?
This clinical trial studies the following conditions: Myopia.
What interventions are being tested in trial NCT00713856?
The interventions under investigation include: Custom PRK with iris registration (PROCEDURE), Conventional PRK (PROCEDURE).
Who is sponsoring clinical trial NCT00713856?
This trial is sponsored by University of Utah, which has 818 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00713856 being conducted?
This trial has 1 study location across Utah. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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Where NCT00713856's enrollment target sits among peer trials
44 78th of 90 higher than 13 of 90 other Myopia trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Myopia 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.
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