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Sponsored by: |
Pfizer |
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Information provided by: | Pfizer |
ClinicalTrials.gov Identifier: | NCT00143429 |
Compare the antihypertensive efficacy of three methods for installing Xalatan
Condition | Intervention | Phase |
---|---|---|
Glaucoma, Open-Angle Ocular Hypertension |
Drug: Xalatan |
Phase II |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Single Blind, Active Control, Crossover Assignment, Safety/Efficacy Study |
Official Title: | Effect Of Corneal Versus Conjunctival Delivery On The Corneal Safety, Tolerability, and Antihypertensive Efficacy Of The Xalatan Ophthalmic Delivery Device |
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Study ID Numbers: | A6111127 |
Study First Received: | September 1, 2005 |
Last Updated: | March 1, 2007 |
ClinicalTrials.gov Identifier: | NCT00143429 |
Health Authority: | United States: Food and Drug Administration |
Primary Open Angle Glaucoma |
Glaucoma Eye Diseases Glaucoma, Open-Angle Vascular Diseases |
Latanoprost Hypertension Ocular Hypertension |
Therapeutic Uses Cardiovascular Diseases Cardiovascular Agents Antihypertensive Agents Pharmacologic Actions |