drugset / Trial / NCT02471105
Investigation of IOP and Tolerability of Bimatoprost 0.01% and Tafluprost Unit Dose Preservative Free 15 Microgram/ml
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Bimatoprost | Other / unclassified | 0.01 % | Topical |
| Subject | Tafluprost | Other / unclassified | 15 ug/ml | Topical |