Recruitment

Recruitment Status
Completed

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

Summary

Conditions
Intermittent Exotropia
Type
Interventional
Design
  • Allocation: N/A
  • Intervention Model: Single Group Assignment
  • Masking: None (Open Label)
  • Primary Purpose: Treatment

Participation Requirements

Age
Between 4 years and 12 years
Gender
Both males and females

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.

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.

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

Tracking Information

NCT #
NCT02131792
Collaborators
Not Provided
Investigators
  • Principal Investigator: Bo Young Chun, M.D Kyungpook National University Hospital
  • Bo Young Chun, M.D Kyungpook National University Hospital