NCT07152964

Brief Summary

This study aims to investigate the clinical correlation between medial rectus tendon width and surgical dose response in esotropic patients undergoing medical rectus recession

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
28

participants targeted

Target at below P25 for all trials

Timeline
5mo left

Started Sep 2025

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress63%
Sep 2025Oct 2026

First Submitted

Initial submission to the registry

August 26, 2025

Completed
6 days until next milestone

Study Start

First participant enrolled

September 1, 2025

Completed
2 days until next milestone

First Posted

Study publicly available on registry

September 3, 2025

Completed
12 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2026

Expected
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2026

Last Updated

September 3, 2025

Status Verified

August 1, 2025

Enrollment Period

1 year

First QC Date

August 26, 2025

Last Update Submit

August 26, 2025

Conditions

Strabismus

Outcome Measures

Primary Outcomes (2)

  • Clinical correlation between medial rectus tendon width and surgical dose response in comitant esotropic patients undergoing medial rectus recession

    Can medial rectus tendon width affect surgical dose response in commitant esotropic patients undergoing medial rectus recession

    Baseline

  • Variation in medial rectus tendon width in different age groups

    Baseline

Interventions

CaliperDEVICE

Measure medial rectus tendon width with caliper intraoperative

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

All patients with comitant esotropia scheduled for unilateral or bilateral medial rectus recession

You may qualify if:

  • \- All patients with comitant esotropia scheduled for unilateral or bilateral medial rectus recession

You may not qualify if:

  • previous extraocular muscle surgery Incomitant esotropia

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Related Links

MeSH Terms

Conditions

Strabismus

Condition Hierarchy (Ancestors)

Ocular Motility DisordersCranial Nerve DiseasesNervous System DiseasesEye Diseases

Study Officials

  • Ali Natag Riad, Professor

    Assiut University

    STUDY DIRECTOR

  • Mohammed Anwr Sayed, Assistant professor

    Assiut University

    STUDY DIRECTOR

  • Sara Hussein AlAttar, Assistant professor

    Assiut University

    STUDY DIRECTOR

Central Study Contacts

Reham Yahya AbdelMohsen, Resident doctor

CONTACT

+201140167502rehamyahya123456@gmail.com

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Resident doctor

Study Record Dates

First Submitted

August 26, 2025

First Posted

September 3, 2025

Study Start

September 1, 2025

Primary Completion (Estimated)

September 1, 2026

Study Completion (Estimated)

October 1, 2026

Last Updated

September 3, 2025

Record last verified: 2025-08