CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 197 enrolled
Drug / intervention
Bilateral lateral rectus recession (BLRc) +1 moreprocedure
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01032603
NCT01032603N/ACompleted
CompareCT.gov

A Randomized Trial of Bilateral Lateral Rectus Recession Versus Unilateral Lateral Rectus Recession With Medial Rectus Resection for Intermittent Exotropia

Jaeb Center for Health Research·interventional·Posted Dec 15, 2009·Updated Feb 7, 2024

In Brief

A clinical study evaluating Bilateral lateral rectus recession (BLRc) and Unilateral lateral rectus recession with medial rectus resection (R&R) for Exotropia. Completed, enrolled 197 participants across 1 site.

Detailed Summary

The purpose of this study is to evaluate the effectiveness of bilateral lateral rectus muscle recession versus unilateral lateral rectus recession with medial rectus resection procedures for the treatment of basic type and pseudo divergence excess type intermittent exotropia.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsExotropia
CountriesUnited States
CollaboratorsPediatric Eye Disease Investigator Group, National Eye Institute (NEI)

Timeline

N/ACompletedFinished
20102011201220132014201520162017201820192020202120222023202420252026
First PostedDec 15, 2009
Enrollment StartJun 1, 2010
Primary CompletionFeb 9, 2017
Study CompletionFeb 18, 2022
TodayJul 2, 2026
Enrollment to primary: 6.7 yearsPosted 16.5 years ago

Interventions

Bilateral lateral rectus recession (BLRc)procedure

Bilateral lateral rectus recession surgery

Unilateral lateral rectus recession with medial rectus resection (R&R)procedure

A unilateral lateral rectus recession combined with a medial rectus resection in the same eye. Choice of eye at investigator discretion based on any interocular difference, position under anesthesia, fixation preference, or forced duction testing. Reason for choice of eye will be recorded.