drugset / Trial / NCT05667454

MAD Trial: Myopia Atropine Dose

NCT05667454

RandomizedParallel-groupQuadruple-blindTreatment

Summary

The goal of this interventional study is to compare the efficacy of Atropine 0.05% to Atropine 0.5% treatment against progression of axial length in European children with progressive myopia, and to evaluate the safety, adherence, and reasons for nonresponse. Subjects will use Atropine eye drops for a period of 3 years, followed by a 2 year observational period.

Timeline

Start
2022-12-19
Primary completion
2029-03-01
Completion
2029-04-01

Drugs

EvaluationDrugModalityDoseRoute
Comparator Atropine Other / unclassified 0.05 % Other
Comparator Atropine Other / unclassified 0.5 % Other

Indications