drugset / Trial / NCT02471105

Investigation of IOP and Tolerability of Bimatoprost 0.01% and Tafluprost Unit Dose Preservative Free 15 Microgram/ml

NCT02471105

RandomizedCrossoverSingle-blindTreatment

Summary

This cross-over study will investigate the efficacy and safety of BIMMD and TUDPF in a clinical setting.

Timeline

Start
2015-09
Primary completion
2017-05
Completion
2017-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Bimatoprost Other / unclassified 0.01 % Topical
Subject Tafluprost Other / unclassified 15 ug/ml Topical