Trials / Completed
CompletedNCT00051194
A 6-week Safety & Efficacy Study of Combination Intraocular Pressure-lowering Therapy in Patients With Open-angle Glaucoma or Ocular Hypertension
A 6-week Safety and Efficacy Study of Combination IOP-lowering Therapy in Patients With Open-angle Glaucoma or Ocular Hypertension.
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- —
- Sponsor
- Alcon Research · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
To compare the intraocular pressure(IOP)-lowering efficacy of morning or evening instillations of a combination IOP-lowering therapy in patients with open-angle glaucoma or ocular hypertension.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Combination IOP Lowering Therapy |
Timeline
- Start date
- 2002-09-01
- Primary completion
- 2003-07-01
- Completion
- 2003-07-01
- First posted
- 2003-01-07
- Last updated
- 2012-04-16
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00051194. Inclusion in this directory is not an endorsement.