Early Results of Slanted Recession of the Lateral Rectus Muscle for Intermittent Exotropia With Convergence Weakness

May 4, 2014 updated by: Bo Young Chun, Kyungpook National University Hospital

Early Results of Slanted Recession of the Lateral Rectus Muscle for Intermittent Exotropia With Convergence Weakness; A Prospective Study

This study was conducted to evaluate results of slanted recession of the lateral rectus muscle for intermittent exotropia with convergence weakness

Study Overview

Status

Completed

Detailed Description

This prospective study included 31 patients who underwent slanted lateral rectus muscle recession for intermittent exotropia with convergence weakness. Measurements of preoperative and postoperative deviation angle, stereopsis was performed.

Study Type

Interventional

Enrollment (Actual)

31

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Kyungsangpookdo
      • Daegu, Kyungsangpookdo, Korea, Republic of, 700-721
        • Bo Young Chun

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

2 years to 10 years (Child)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Patients with intermittent exotropia greater at near than at distance by 10 prism diopters or more
  • Patients with follow up duration greater than 6 months

Exclusion Criteria:

  • Patients with previous ocular or strabismus surgery
  • Patients with ocular or neurologic pathologic conditions
  • Follow up duration less than 6 months

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Lateral Rectus Muscle Slanted Recession
Slanted recession of the lateral rectus muscle for the intermittent exotropia with convergence weakness
All patients who had intermittent exotropia with convergence weakness was enrolled to the slanted lateral rectus muscle recession group.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Changes from baseline of exodeviations angle after slanted recession surgery at 6 months.
Time Frame: preop, 6months postop
Measurement of deviation angle after slanted recession surgery was performed.
preop, 6months postop

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Changes from baseline of near-distance difference after slanted recession surgery at 6 months
Time Frame: preop, 6 months postop
Measurement of stereopsis after slanted recession was performed.
preop, 6 months postop

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Bo Young Chun, M.D, Kyungpook National University Hospital

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

June 1, 2010

Primary Completion (Actual)

June 1, 2012

Study Completion (Actual)

April 1, 2014

Study Registration Dates

First Submitted

May 4, 2014

First Submitted That Met QC Criteria

May 4, 2014

First Posted (Estimate)

May 6, 2014

Study Record Updates

Last Update Posted (Estimate)

May 6, 2014

Last Update Submitted That Met QC Criteria

May 4, 2014

Last Verified

May 1, 2014

More Information

Terms related to this study

Other Study ID Numbers

  • KNUH2014-02

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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