drugset / Trial / NCT06077682

Cycloplegic Refraction in Pediatric Patients With Esotropia

NCT06077682

RandomizedCrossoverTriple-blindTreatment

Summary

The primary outcome of this study is to compare cyclopentolate 1% and tropicamide 1% for cycloplegic refractions in pediatric populations with esotropia. This will be a prospective double-blinded randomized clinical trial (RCT), multi-center, with randomized sequencing of cycloplegic agent; each patient received one agent at one visit, and the other agent in the next visit (2 different visits ≥ 1 week apart) within 3 months.

Timeline

Start
2023-09-01
Primary completion
2024-09-01
Completion
2024-12-01

Drugs

EvaluationDrugModalityDoseRoute
Comparator cyclopentolate Unknown 1 % Other
Comparator tropicamide Small molecule 1 % Other