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Terminated Not applicable Interventional

Evaluation of Exotropia After Patching the Eye or After Prism Adaptation

ClinicalTrials.gov ID: NCT05242510

Public ClinicalTrials.gov record NCT05242510. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 5, 2026, 11:05 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Divergence Excess/Simulated Divergence Excess Exotropia (DESDEE)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT05242510
Recruitment status
Terminated
Study type
Interventional
Phase
Not applicable
Lead sponsor
University of Rochester
Other
Enrollment
1 participant

Conditions and interventions

Conditions

Interventions

Procedure

Eligibility (public fields only)

Age range
Up to 17 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 26, 2024
Primary completion
Sep 17, 2024
Completion
Sep 17, 2024
Last update posted
Apr 3, 2025

2024

United States locations

U.S. sites
5
U.S. states
4
U.S. cities
5
Facility City State ZIP Site status
University of California Los Angeles Los Angeles California 90095
Harvard University Boston Massachusetts 02115
Ross Eye Institute Buffalo New York 14209
University of Rochester Medical Center Rochester New York 14642
University of Pittsburgh Pittsburgh Pennsylvania 15213

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 4 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05242510, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 3, 2025 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05242510 live on ClinicalTrials.gov.

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