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Sponsored by: |
Merck |
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Information provided by: | Merck |
ClinicalTrials.gov Identifier: | NCT00140907 |
A study to determine the renal protective effect (measured as an incidence of chronic allograft nephropathy)of losartan in patients after renal transplant.
Condition | Intervention | Phase |
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Renal Disorder |
Drug: MK0954, losartan potassium/Duration of Treatment: 2 years Drug: Comparator: placebo / Duration of Treatment: 2 years |
Phase IV |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Efficacy Study |
Official Title: | Extension Study Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Renal Protective Effects of Losartan in Patients With Renal Transplants |
Estimated Enrollment: | 420 |
Study Start Date: | April 2000 |
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Study ID Numbers: | 2005_053 |
Study First Received: | August 30, 2005 |
Last Updated: | October 25, 2005 |
ClinicalTrials.gov Identifier: | NCT00140907 |
Health Authority: | Spain: Ministry of Health |
Losartan Urologic Diseases Kidney Diseases Angiotensin II |
Angiotensin II Type 1 Receptor Blockers Molecular Mechanisms of Pharmacological Action Therapeutic Uses Cardiovascular Agents |
Anti-Arrhythmia Agents Antihypertensive Agents Pharmacologic Actions |