drugset / Trial / NCT02802137
24-hour Efficacy and Ocular Surface With Talfuprost and Triple Combined Therapy
RandomizedCrossoverSingle-blindTreatment
Summary
The study investigated the 24-hour efficacy and ocular surface health with preservative-free tafluprost and a combined preservative-free regimen (tafluprost and dorzolamide/timolol fixed combination) in open-angle glaucoma patients insufficiently controlled on latanoprost monotherapy and showing signs, or symptoms of ocular surface disease with preservative-containing latanoprost monotherapy. This trial randomized open-angle glaucoma patients insufficiently controlled (IOP \> 20 mm Hg) on branded, or generic latanoprost monotherapy who required further IOP reduction and who demonstrated clinical signs, or symptoms of ocular surface disease.
Timeline
- Start
- 2015-03
- Primary completion
- 2015-12
- Completion
- 2016-01
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Dorzolamide | Small molecule | — | Topical |
| Comparator | Tafluprost | Other / unclassified | — | Topical |
| Comparator | Timolol | Other / unclassified | — | Topical |