Trials / Completed
CompletedNCT01298687
Divided Dose of TRAVATAN®
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 67 (actual)
- Sponsor
- Alcon Research · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to compare the incremental dosing of travoprost ophthalmic solution versus once a day dosing of TRAVATAN® in lowering intraocular pressure (IOP) in patients with open-angle glaucoma (OAG) or ocular hypertension (OHT).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Travoprost Ophthalmic Solution, 0.00013% | Cumulative daily dose is below the travoprost ophthalmic solution, 0.004% once daily dose |
| DRUG | Travoprost Ophthalmic Solution, 0.00033% | Cumulative daily dose equals the travoprost ophthalmic solution, 0.004% once daily dose |
| DRUG | Travoprost Ophthalmic Solution, 0.001% | Cumulative daily dose is above the travoprost ophthalmic solution, 0.004% once daily dose |
| DRUG | Travoprost Ophthalmic Solution, 0.00267% | Cumulative daily dose is above the travoprost ophthalmic solution, 0.004% once daily dose |
| DRUG | Travoprost Ophthalmic Solution, 0.004% | |
| DRUG | Travoprost Vehicle | Inactive ingredients used as an active comparator |
Timeline
- Start date
- 2011-02-01
- Primary completion
- 2011-04-01
- Completion
- 2011-04-01
- First posted
- 2011-02-18
- Last updated
- 2017-05-05
Source: ClinicalTrials.gov record NCT01298687. Inclusion in this directory is not an endorsement.