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Bilateral Lateral Rectus Recession Versus Bilateral Primary Medial Rectus Resection in Intermittent Exotropia

Comparison Between Bilateral Lateral Rectus Recession and Bilateral Primary Medial Rectus Resection in Basic Type Intermittent Exotropia

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06650735
Enrollment
40
Registered
2024-10-21
Start date
2023-07-01
Completion date
2024-11-30
Last updated
2024-10-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Intermittent Exotropia

Keywords

IXT, lateral rectus recession, medial rectus resection

Brief summary

The goal of this clinical trial is to compare the efficacy of bilateral lateral rectus recession and bilateral primary medial rectus resection in basic type intermittent exotropia Participants will be randomized into two groups: bilateral lateral rectus (BLR) recession and bilateral medial rectus (BMR) resection groups then followed up in the clinic for 6 months to compare motor alignment and sensory functions

Detailed description

Study location: Cairo university hospitals Methodology: Patients with basic type intermittent exotropia who are indicated to undergo surgical intervention will be grouped into two groups one group will undergo bilateral lateral rectus recession and the other will undergo bilateral medial rectus resection. * Preoperatively, all patients will be subjected to: 1. A detailed history taking including presence of asthenopia, monocular closure, disfigurement or diplopia. The previous use of glasses for optical correction, use of minus lenses, or prior part time occlusion will be documented. 2. A detailed ophthalmological examination; including uncorrected and best corrected visual acuity whenever possible, cycloplegic refraction, anterior segment examination and dilated fundus examination. 3. Motor Evaluation: * Ductions and versions will be done to assess the ocular motility in 9 positions of gaze. * The angle of deviation will be measured by the alternate prism cover test for both distance (6 meters) and near (33 cm) , with and without glasses. * The angles of misalignment will also be measured in side gazes and in straight up and down gaze whenever possible. * In patients with near-far disparity, the angle of deviation will be measured again after patching one eye for 30 minutes, as well as after putting +3 D lenses in front of each eye. Patients with near-far disparity \>10 prism diopters (PD) will not be included 4. Sensory Evaluation: Worth 4 dot test and stereopsis using Random dot test (when possible) The control of exotropia will be assessed using both the newcastle control score Patients will be randomly assigned to either surgery using simple randomization by random number generator * Intervention: * One group will undergo bilateral lateral rectus recession and the other will undergo bilateral medial rectus resection according to the standard tables. * All cases will be done under general anaesthesia. * Both surgeries take about 30 minutes. * Postoperative treatment combined tobramycin 0.3% and dexamethasone 0.1% eye drops 3 times daily and the same combination eye ointment at night for 3 weeks. * Postoperative follow up will be 1 week, 6 weeks, 3 months and 6 months (minimum follow up) * Postoperative assessment: * Extraocular movement in lateral gazes will be examined for comitance * Alignment in the primary position will be assessed and any deviation will be measured using alternate prism cover test * Palpebral fissure height will be measured * Worth 4 dot test and stereopsis will be assessed (when possible) * In cases of failure either over correction or under correction reoperation will be performed after 3 months of the initial surgery. * Sample size We are planning a study of the difference in the postoperative angle between the 2 surgical techniques. Assuming a mean difference of 5 PD with a standard deviation of 5 PD, an alpha error of 0.05 and a power of study of 0.8, a total of 17 subjects were found to be needed in each group. Assuming a drop-out rate of 20%, a sample of 20 subjects will be targeted in each group.

Interventions

PROCEDUREBMR resection

Lid speculum will be applied. Fornix conjunctival incision will be used to expose medial rectus muscle. Area that will be resected will be marked using calipers. Double-armed polyglactin 910 suture (6/0 Vicryl) will be used in securing the muscle. The muscle then excised anterior to the sutures and the stump cut flush to the sclera. The muscle will be sutured again to the original insertion by scleral sutures which will be tied together. Conjunctiva will be closed using polyglactin 910 suture (6/0 Vicryl).

PROCEDUREBLR recession

Lid speculum will be applied. Fornix conjunctival incision will be used to expose lateral rectus muscle. Double-armed polyglactin 910 suture (6/0 Vicryl) will be used in securing the muscle close to the insertion. The muscle will then be cut anterior to the sutures flush with the sclera. Calipers will used to mark the new insertion on sclera measured from the stump. The muscle will be sutured again to the new insertion by scleral sutures, which will be tied together. Conjunctiva will be closed using polyglactin 910 suture (6/0 Vicryl).

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
5 Years to 30 Years
Healthy volunteers
No

Inclusion criteria

* Patients with basic type intermittent exotropia * Measurable angle 25-40 prism diopters

Exclusion criteria

* Restrictive or paralytic deviation or if forced duction test is positive on horizontal muscles * Incomitant deviation, vertical or oblique muscles surgery and significant A or V pattern * Previous strabismus, orbital or buckle surgery

Design outcomes

Primary

MeasureTime frameDescription
Motor alignment in primary position12 monthsSuccess rate defined as orthophoria between exotropia/phoria ≤ to 8 prism diopters & esotropia/phoria ≤ 4 prism diopters

Secondary

MeasureTime frameDescription
Palpebral fissure height12 monthsChange in palpebral fissure height in mm
Lateral gaze comitance/incomitance12 monthsDifference between angles of deviation in right gaze, primary position, and left gaze
Stereopsis12 monthsChange in stereoacuity in log seconds of arc

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026