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NCT00889941 · ClinicalTrials.gov registry record · Phase 4

Effect of Preoperative Pupil Size on Quality of Vision After Wavefront-Guided LASIK

A Phase 4 study of Myopia, sponsored by Stanford University.

Completed
Registry status
Phase 4
Development phase
51
Enrollment target
1
Study location

NCT00889941 is a Phase 4 study of Myopia that has completed, run by Stanford University. The registered enrollment target is 51 participants, below the 267-participant average among 90 other Myopia trials with a reported enrollment target (81% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT00889941, a Phase 4 study of Myopia, has completed, sponsored by Stanford University.

COMPLETED
Registry status
Phase 4
Development phase
51 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to evaluate whether the size of the pupil has an effect on quality of vision in patients undergoing LASIK surgery.

Conditions Studied

Interventions

  • PROCEDURE LASIK

Study Locations (1)

California

  • Stanford University School of Medicine - Stanford

Trial Details

FieldValue
Enrollment Target 51 participants
Start Date 2004-05
Est. Completion 2005-11
Phase Phase 4

Sponsor

Stanford University

1,744 total trials

What the Registry Record Tells You About NCT00889941

The ClinicalTrials.gov registry entry for NCT00889941 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 51 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 (81% lower). The listed sponsor is Stanford University, which has 1,744 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Myopia appearing as the primary indexed condition, and to 1 intervention - of which LASIK is the first listed.

NCT00889941 reports 1 study location spanning 1 distinct geographic area - top geographies include California.

Frequently Asked Questions

What is clinical trial NCT00889941 about?

NCT00889941 is a clinical study titled "Effect of Preoperative Pupil Size on Quality of Vision After Wavefront-Guided LASIK". The purpose of this study is to evaluate whether the size of the pupil has an effect on quality of vision in patients undergoing LASIK surgery.

What is the current status of trial NCT00889941?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 51 participants. The study started on 2004-05. Estimated completion is 2005-11.

What conditions does trial NCT00889941 study?

This clinical trial studies the following conditions: Myopia.

What interventions are being tested in trial NCT00889941?

The interventions under investigation include: LASIK (PROCEDURE).

Who is sponsoring clinical trial NCT00889941?

This trial is sponsored by Stanford University, which has 1,744 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00889941 being conducted?

This trial has 1 study location across California. 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 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.