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| Sponsor: | Alcon Research |
|---|---|
| Information provided by: | Alcon Research |
| ClinicalTrials.gov Identifier: | NCT00051142 |
Purpose
The purpose of this study is to evaluate the safety and IOP-lowering efficacy of Travoprost (0.004%) compared to Latanoprost (0.005%) in patients with chronic open-angle glaucoma or ocular hypertension.
| Condition | Intervention | Phase |
|---|---|---|
|
Glaucoma, Open-Angle Ocular Hypertension |
Drug: Travoprost Drug: Latanoprost |
Phase III |
| Study Type: | Interventional |
| Study Design: | Treatment, Randomized, Double-Blind, Active Control, Parallel Assignment, Safety/Efficacy Study |
| Official Title: | A Safety and Efficacy Study of Travoprost 0.004% Compared to Latanoprost 0.005% in Patients With Open-Angle Glaucoma or Ocular Hypertension |
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Adult patients of any race and either sex with open-angle glaucoma (with or without pigment dispersion or pseudoexfoliation component) or ocular hypertension.
Contacts and Locations
More Information
| Study ID Numbers: | C-01-36 |
| Study First Received: | January 3, 2003 |
| Last Updated: | August 4, 2008 |
| ClinicalTrials.gov Identifier: | NCT00051142 History of Changes |
| Health Authority: | United States: Food and Drug Administration |
|
Glaucoma POAG OAG OHT |
|
Eye Diseases Vascular Diseases Cardiovascular Agents Latanoprost Antihypertensive Agents Pharmacologic Actions Travoprost |
Glaucoma Glaucoma, Open-Angle Therapeutic Uses Cardiovascular Diseases Hypertension Ocular Hypertension |