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NCT07294599

Morning Versus Evening Patching in Childhood Amblyopia

Not yet recruiting NA Last updated 26 December 2025
What this trial tests

NA trial testing eye-patching in Amblyopia in 100 participants. Not yet recruiting.

Timeline
14 December 2025
Primary endpoint
14 June 2026
14 June 2026

Quick facts

Lead sponsorYarmouk University
PhaseNA
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposeother
Enrollment100
Start date14 December 2025
Primary completion14 June 2026
Estimated completion14 June 2026

Drugs / interventions tested

Conditions studied

Sponsor

Yarmouk University

Who can join

Adults 4 to 8, any sex, with Amblyopia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

To determine whether the time of day at which daily occlusion (patching) is administered - morning (08:00-10:00) versus evening (17:00-19:00) - affects the amount of visual-acuity improvement in the amblyopic eye in children with unilateral amblyopia. Rationale: While occlusion therapy remains the mainstay for treatment of childhood amblyopia, existing trials have focused on patching duration, not on the timing of occlusion. Diurnal or chronobiological factors - such as fluctuations in neuroplasticity, attention, compliance, or visual demand during the day - may influence the efficacy of patching. Understanding whether timing matters could help optimize occlusion therapy, improve outcomes, and reduce treatment burden.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Amblyopia

Currently open trials in the same condition.

Other Yarmouk University trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07294599.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing