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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 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.

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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

Myopia

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

FieldValue
Enrollment Target 44 participants
Start Date 2007-11
Est. Completion 2010-05
Phase NA

Sponsor

University of Utah

818 total trials

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What the Registry Record Tells You About NCT00713856

The ClinicalTrials.gov registry entry for NCT00713856 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 44 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 267-participant average among 90 other Myopia trials with a reported enrollment target (84% lower). The listed sponsor is University of Utah, which has 818 total studies on file at ClinicalTrials.gov.

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 1 study location spanning 1 distinct geographic area - top geographies include 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.

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

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.