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Exotropia clinical trials

View clinical trials related to Exotropia.

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NCT ID: NCT06117813 Recruiting - Clinical trials for Intermittent Exotropia

Visual Perceptual Learning Based Digital Therapeutics for Stereopsis in Intermittent Exotropia

Start date: December 22, 2023
Phase: N/A
Study type: Interventional

This study evaluates the efficacy and safety of visual perceptual learning for improving stereopsis in intermittent exotropia. Half of participants will receive visual perceptual training using the Nu.T. The other half will not receive any training because there is no standard treatment for decreased stereopsis in intermittent exotropia.

NCT ID: NCT05615519 Recruiting - Strabismus Clinical Trials

Validation of a Smartphone-based Intelligent Diagnosis and Measurement for Strabismus

Start date: December 2, 2022
Phase:
Study type: Observational

The current measurement methods of strabismus include the corneal light reflection method, prism alternate covering, etc., which especially rely on the subjective experience of doctors, and there is a large error between different measurers, leading to serious underestimation of strabismus prevalence and insufficient care for strabismus patients. Here, the investigators established and validated an artificial intelligence system to achieve an automatic diagnosis of strabismus based on patient-sourced videos of programmatic cover tests. Three-dimensional reconstruction methods are used to digitize the parameters of head and eye positions. This system has been integrated into a smartphone platform to be further validated through hospital-based and population-based clinical trials.

NCT ID: NCT05462821 Recruiting - Clinical trials for Intermittent Exotropia

Full-Time Occlusion Therapy for Intermittent Exotropia in Children

IXT7
Start date: November 21, 2022
Phase: N/A
Study type: Interventional

Determine whether full-time patching is more effective than observation for improving distance control of IXT after 3 months of treatment (on-treatment outcome).

NCT ID: NCT05379855 Recruiting - Myopia Clinical Trials

A-eyedrops on Ocular Alignment and Binocular Vision

Start date: March 2, 2024
Phase: N/A
Study type: Interventional

Atropine is a non-selective muscarinic acetylcholine (M) receptor antagonist that paralyzes the ciliary muscle, dilates the pupil, and reduces the power of accommodation. Current studies have confirmed the effect of low concentrations of atropine drops in slowing the progression of myopia. In the atropine treatment for myopia (ATOM2) study, there was a rapid and dose-dependent decrease in accommodation after atropine drops: after 2 weeks of use, accommodation decreased from baseline 16.2D to 11.3D (4.9D) in the 0.01% atropine drops group, from baseline 16.7D to 3.8D (12.9D) in the 0.1% atropine group, and from baseline 15.8 D to 2.2 D (13.6 D) in the 0.5% atropine group; one year after withdrawal, there was some recovery of the accommodation in all the three groups, but it was still lower than the baseline values for each group, with a mean decrease of 2.56 D.Similar results were found in the Low-concentration Atropine for Myopia Progression (LAMP) Study by Janson C. Yam, 0.05% atropine drops reduced the accommodation by approximately 2D on average after 1 year of treatment. In general, if accommodation decreases by 2D or more compared to normal values, accommodation insufficiency is considered. There is a linkage between accommodation and convergence called accommodative convergence-to-accommodation (AC/A) which is closely related to exotropia. It was reported that the amount of accommodation required to maintain binocular fusion in patients with intermittent exotropia was greater than that of normal controls. In addition, pupil size and visual acuity are also factors that affect accommodation. In summary, the reduced accommodation amplitude, pupil dilation, and blurred near vision caused by atropine drops would affect the progression of intermittent exotropia and the ocular alignment after the surgery. In most cases, the reduced accommodation and convergence might induce exotropia, but in some patients, they may use more accommodative stimuli to compensate the insufficiency of accommodation, and there may be an increase in convergence or even esotropia. Taken together, due to the effect of atropine drops on pupil size, near visual acuity, and accommodation amplitude, the investigators hypothesize that atropine drops are likely to affect binocular vision and ocular alignment in patients with exotropia and exophoria.

NCT ID: NCT05242510 Recruiting - Exotropia Clinical Trials

Evaluation of Exotropia After Patching the Eye or After Prism Adaptation

DESDEE
Start date: December 1, 2024
Phase: N/A
Study type: Interventional

This study intends to determine the number and percent of subjects initially diagnosed with divergence excess exotropia which would be reclassified as simulated divergence excess exotropia if tested after 24 hours of monocular occlusion (patching) or after prism adaptation for the distance angle.

NCT ID: NCT05234957 Recruiting - Clinical trials for Intermittent Exotropia

Symmetric vs Asymmetric BLR Recession in Management of Basic IXT With Ocular Dominance

Start date: April 17, 2022
Phase: N/A
Study type: Interventional

The study aims to investigate ocular motor and sensory outcomes of two different strategies of lateral rectus recession; symmetric and asymmetric, in management of basic type intermittent exotropia with ocular dominance.

NCT ID: NCT04487249 Recruiting - Clinical trials for Intermittent Exotropia

Trial of Vision Therapy for Intermittent Exotropia

VT-IXT
Start date: October 1, 2021
Phase: N/A
Study type: Interventional

The main objective of this randomized trial comparing vision therapy to observation is to determine the short-term effectiveness of vision therapy on distance intermittent exotropia control. The results will help determine whether to proceed to a full-scale, long-term randomized trial.

NCT ID: NCT04308538 Recruiting - Clinical trials for Alternating Exotropia

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

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

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

NCT ID: NCT04199871 Recruiting - Clinical trials for Intermittent Exotropia

Improving Control of Alignment in Intermittent Exotropia

Start date: March 25, 2021
Phase: N/A
Study type: Interventional

Aim 1: To determine whether use of dichoptic movies for 4 weeks may be helpful in improving control of alignment in children with intermittent exotropia (IXT), thus allowing IXT to be managed non-surgically Aim 2: To determine pre-IXT surgery use of dichoptic movies for 4 weeks post-operatively may be helpful in maintaining successful control of alignment in children who have surgical correction of IXT

NCT ID: NCT02902887 Recruiting - Clinical trials for Intermittent Exotropia

Monitored Controlled Intermittent Alternate Occlusion (CIAO) Therapy for Intermittent Exotropia

Start date: August 2016
Phase: N/A
Study type: Interventional

This study presents an opportunity to understand a novel, previously unreported controlled intermittent alternate occlusion (CIAO) therapy glasses, which may improve the control of Intermittent exotropia (IXT).