- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02131792
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
Conditions
Intervention / Treatment
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
-
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Kyungsangpookdo
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Daegu, Kyungsangpookdo, Korea, Republic of, 700-721
- Bo Young Chun
-
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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.
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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
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Measurement of deviation angle after slanted recession surgery was performed.
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preop, 6months postop
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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
Additional Relevant MeSH Terms
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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-
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-
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-
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-
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