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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02131792
Other study ID # KNUH2014-02
Secondary ID
Status Completed
Phase N/A
First received May 4, 2014
Last updated May 4, 2014
Start date June 2010
Est. completion date April 2014

Study information

Verified date May 2014
Source Kyungpook National University
Contact n/a
Is FDA regulated No
Health authority Korea: Institutional Review Board
Study type Interventional

Clinical Trial Summary

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


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.


Recruitment information / eligibility

Status Completed
Enrollment 31
Est. completion date April 2014
Est. primary completion date June 2012
Accepts healthy volunteers No
Gender Both
Age group 4 Years to 12 Years
Eligibility 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 Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
Slanted recession of the lateral rectus muscle
All patients who had intermittent exotropia with convergence weakness was enrolled to the slanted lateral rectus muscle recession group.

Locations

Country Name City State
Korea, Republic of Bo Young Chun Daegu Kyungsangpookdo

Sponsors (1)

Lead Sponsor Collaborator
Kyungpook National University

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Changes from baseline of exodeviations angle after slanted recession surgery at 6 months. Measurement of deviation angle after slanted recession surgery was performed. preop, 6months postop No
Secondary Changes from baseline of near-distance difference after slanted recession surgery at 6 months Measurement of stereopsis after slanted recession was performed. preop, 6 months postop No
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