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Bil. LR Rec. Using Standard Tables VS Reduced Numbers in Intermittent Exo. in Children Under 6

Bilateral Lateral Rectus Recession Using Standard Tables Versus Bilateral Lateral Rectus Recession Using Modified Reduced Numbers in Intermittent Exotropia in Children Less Than 6 Years Old

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04308538
Enrollment
100
Registered
2020-03-16
Start date
2020-04-01
Completion date
2022-04-30
Last updated
2020-03-16

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

Conditions

Alternating Exotropia

Brief summary

comparing the motor alignment and the incidence of postoperative esotropia following the correction of intermittent exotropia in children below 7 years by bilateral lateral rectus recession using the standard recession tables postulated by Parks versus correction using a reduced recession by one millimeter

Interventions

PROCEDUREStandard Recession

Bilateral lateral rectus muscle recession will be performed through fornix approach using standard tables

PROCEDUREReduced Recession

Bilateral lateral rectus muscle recession will be performed through fornix approach using reduced numbers

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
2 Years to 6 Years
Healthy volunteers
No

Inclusion criteria

* Patients with poor control intermittent exotropia (where poor control is defined as having a Newcastle score of 3 or more). (9) * Basic, pseudo- divergence excess and divergence excess types are included. * If associated with amblyopia it should be corrected before the surgical correction (where the visual acuity will be assessed by the single crowded HOTV test using a commercial projector).

Exclusion criteria

* Intermittent exotropia of the convergence insufficiency type. * Intermittent exotropia with angle of deviation greater than 50 prism diopters. * Patients with previous squint surgery. * Patients with secondary deviation due to a sensory lesion or neurological condition.

Design outcomes

Primary

MeasureTime frameDescription
Motor success rate6 monthsNumber of patients with orthophoria (8 PD exophoria to 4 PD esophoria)

Secondary

MeasureTime frameDescription
Pattern strabismus6 monthsNumber of patients who develop pattern strabismus

Countries

Egypt

Contacts

Primary ContactAhmed Awadein, MD
ahmedawadein@yahoo.com+201223911743
Backup ContactDina Hassanein, MD
drdhossam@yahoo.com+20 100 517 2781

Outcome results

None listed

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