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Inferior Oblique Muscle Anteriorization Versus Anteriorization and Resection in DVD With IOOA

NCT05980962 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 54

Last updated 2023-08-08

No results posted yet for this study

Summary

The goal of this clinical trial is to compare the results of two surgical modalities in patients with Dissociated vertical deviation with inferior oblique muscle overaction . The main questions it aims to answer are:

* How much does the magnitude of DVD improve after each modality?
* Is the IOOA eliminated? Participants will be divided into two equal groups; Researchers will compare the efficacy of symmetrical anteriorization of the inferior oblique and adding an additional rescetion to one eye in the second group to see which group had more signifcant reduction in the magnitude of DVD and IOOA.

Conditions

  • Dissociated Vertical Deviation
  • Inferior Oblique Overaction

Interventions

PROCEDURE

Inferior oblique anteriorization

symmterical anteriorization the the inferior oblique muscle 1 mm behind and lateral to the inferior rectus insertion

PROCEDURE

Inferior oblique anteriorization together with unliateral resction

asymmterical surgery, anteriorization the the inferior oblique muscle 1 mm behind and lateral to the inferior rectus insertion in one eye, and an additional 3-5 mm resction of the inferior oblique in the eye with the larger devation

Sponsors & Collaborators

  • Kasr El Aini Hospital

    lead OTHER

Principal Investigators

  • Hala M. Elhiliali · Cairo University

  • Magda S. Abdel-Aziz · Cairo University

  • Heba M. Fouad · Cairo University

  • Ghada O. Mohamed · Cairo University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
1 Year
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-12-01
Primary Completion
2021-12-31
Completion
2022-07-15

Countries

  • Egypt

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05980962 on ClinicalTrials.gov