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Exotropia clinical trials

View clinical trials related to Exotropia.

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NCT ID: NCT05786053 Completed - V Pattern Esotropia Clinical Trials

Correction of V-pattern Strabismus by Graded Recession of Inferior Oblique Muscle .

Pattern
Start date: October 1, 2020
Phase: N/A
Study type: Interventional

V pattern strabismus is the commonest of alphabet pattern. Its identification is essential to plan a proper surgical management. Graded recession is a very logical approach to treat inferior oblique overaction (IOOA). The aim Is to evaluate the efficacy of graded recession of inferior oblique muscle for correction of different grades of V pattern.

NCT ID: NCT05643456 Completed - Exotropia Clinical Trials

Surgery for Large Angle Exotropia Two Muscles Versus Three Muscles

XT
Start date: July 1, 2020
Phase: N/A
Study type: Interventional

Comparison Between The Results Of Two Muscles Surgery And Three Muscles Surgery For The Treatment Of Large Angle Exotropia

NCT ID: NCT04961021 Completed - Strabismus Clinical Trials

Management of Consecutive Exotropia

Start date: August 3, 2020
Phase: N/A
Study type: Interventional

Patients with consecutive exotropia will be managed by medial rectus muscle advancement +/- resection or medial rectus muscle advancement +/- lateral rectus recession

NCT ID: NCT04901533 Completed - Exophoria Clinical Trials

Cervical Manipulation (OAA Technique) in Exophories

Start date: May 20, 2021
Phase: N/A
Study type: Interventional

Objetive: to assess the efficacy of the occipito-atlas-axis cervical manipulation technique to correct ocular divergence in subjects with exophoria. Design: quantitative, experimental, longitudinal and prospective study. Subjects: subjects over 18 years of age, with exophorias, without heterotropies and who do not present a contraindication to cervical manipulation. Methods:Subjects with this ocular mobility dysfunction are going to be evaluated objectively with the Alternate Cover Test. The ocular deviation will be measured at 40 cm and at 4 meters. The individuals who were part of the experimental group underwent the OAA manipulation technique, and to those who were part of the control group a placebo maneuver. Two measurements were taken from this moment, one immediately after the execution of the technique and another one week later.

NCT ID: NCT04286945 Completed - Clinical trials for Surgical Procedure, Unspecified

Lateral Rectus Muscle Tendon Elongation

Start date: January 1, 2017
Phase: N/A
Study type: Interventional

To evaluate a technique using resected medial rectus muscle transplantation for elongation of Lateral rectus tendon as a monocular surgery for large angle sensory exotropia.

NCT ID: NCT04152122 Completed - Clinical trials for Dynamic Stereopsis in Intermittent Exotropia Patients

A Novel Dynamic Random-dot Stereopsis Assessment to Measure the Stereopsis in Intermittent Exotropia

Start date: February 1, 2017
Phase:
Study type: Observational

A novel dynamic random-dot stereopsis test that included motion + disparity (MD), motion (M), and disparity (D), in which the disparity cues range from 200 to 1200 arc-seconds was used. The characteristics of preoperative dynamic stereopsis in 83 intermittent exotropia patients and its associations with clinical features were analysed, and the prognosis was followed up on the 1st day and 2nd, 6th and 12nd months postoperatively.

NCT ID: NCT04064112 Completed - Clinical trials for Convergence Insufficiency Intermittent Exotropia (CI-IXT)

S-BLR Versus C-BLR for CI-IXT in Children

SCCIXT
Start date: October 18, 2019
Phase: N/A
Study type: Interventional

This is a multi-center, randomized single-blind controlled trial to compare the effectiveness of S-BLR with C-BLR for the treatment of CI-IXT in children. Specific Aim 1 (Primary): To compare the surgical successful rate of S-BLR with C-BLR for the treatment of CI-IXT in children. Specific Aim 2 (Secondary): To study the suboptimal surgical outcomes between S-BLR and C-BLR for the treatment of CI-IXT in children.

NCT ID: NCT03998670 Completed - Clinical trials for Exotropia Intermittent

Base-in Prism Spectacles for Intermittent Exotropia

IXT6
Start date: September 1, 2019
Phase: N/A
Study type: Interventional

The objective of this short-term, pilot randomized trial comparing spectacles with relieving prism to spectacles without prism is to determine whether to proceed to a full-scale, longer-term randomized trial. This decision will be based primarily on assessing the initial (8-week) response to prism by comparing treatment groups on the following outcomes: - Mean distance intermittent exotropia (IXT) control score (the mean of 3 control scores) (primary outcome) - The proportion of participants demonstrating a "treatment response," defined as ≥1 point improvement in the mean distance IXT control score without spontaneous exotropia during control testing (secondary outcome) - The proportion of participants reporting adverse effects and good/excellent spectacle wear compliance

NCT ID: NCT03661476 Completed - Clinical trials for Intermittent Exotropia

The Effect of Oculo-Motor Exercises in Intermittent Exotropia

Start date: August 13, 2018
Phase: N/A
Study type: Interventional

In childhood strabismus, exotropia is most frequently seen with intermittent exotropia and convergence failure in the first decade of life. This situation adversely affects children's psychosocial development and creates worries about personal relationships and work life in their future lives. Patients' hesitant attitudes towards surgical treatment led to the out-of-surgery techniques such as exercise therapy. No studies have been found in the literature on the efficancy of the intermittent exotropia treatments with oculo-motor exercises. In our study, it was aimed to investigate the effects of oculo-motor exercises on intermittent exotropia in children.

NCT ID: NCT03153423 Completed - Strabismus Clinical Trials

Basic Intermittent Exotropia and Risk Factors for Postoperative Overcorrection and Under Correction

Start date: August 5, 2017
Phase: N/A
Study type: Interventional

To evaluate preoperative risk factors for overcorrection and undercorrection following surgery for basic intermittent exotropia such as axial length of the globe, refractive error, age and sex