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| Sponsor: | Alcon Research |
|---|---|
| Information provided by: | Alcon Research |
| ClinicalTrials.gov Identifier: | NCT00051181 |
Purpose
To demonstrate that the intraocular pressure(IOP)-lowering efficacy of Travoprost (0.004%) is equal or better than that of Latanoprost 0.005% in patients with chronic angle-closure glaucoma.
| Condition | Intervention | Phase |
|---|---|---|
|
Glaucoma, Angle-Closure Ocular Hypertension |
Drug: Travoprost (0.004%) Drug: Latanoprost (0.005%) |
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 Chronic Angle-Closure Glaucoma. |
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 chronic angle-closure glaucoma.
Contacts and Locations
More Information
| Study ID Numbers: | C-01-38 |
| Study First Received: | January 3, 2003 |
| Last Updated: | August 4, 2008 |
| ClinicalTrials.gov Identifier: | NCT00051181 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 Therapeutic Uses Cardiovascular Diseases Glaucoma, Angle-Closure Hypertension Ocular Hypertension |