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Antiproteinuric Efficacy of Losartan Potassium in Patients with Non-Diabetic Proteinuric Renal Diseases - Article


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Diclofenac Potassium

Cataflam 



Clinical Trial: Antiproteinuric Efficacy of Losartan Potassium in Patients with Non-Diabetic Proteinuric Renal Diseases

This study is no longer recruiting patients.

Sponsored by: Merck
Information provided by: Merck
ClinicalTrials.gov Identifier: NCT00140985

Purpose

Antiproteinuric Efficacy of Losartan Potassium in Patients with Non-Diabetic Proteinuric Renal Diseases.
Condition Intervention Phase
Renal disorder
  Drug: MK0954, losartan potassium
 Phase IV

MedlinePlus related topics:  Kidney Diseases

Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Active Control, Parallel Assignment, Efficacy Study

Further Study Details: 

Study start: January 2000

Eligibility

Ages Eligible for Study:  18 Years and above,  Genders Eligible for Study:  Both
Criteria

Inclusion Criteria:

  • Males or females at least 18 years of age with non-diabetic proteinuric renal diseases

Location Information


Spain
      Merck Sharp & Dohme De Espana, S.A.E., Madrid,  28027,  Spain

Study chairs or principal investigators

Medical Monitor,  Study Director,  Merck   

More Information

Study ID Numbers:  2005_058
Last Updated:  August 31, 2005
Record first received:  August 30, 2005
ClinicalTrials.gov Identifier:  NCT00140985
Health Authority: Spain: Ministry of Health
ClinicalTrials.gov processed this record on 2005-09-13


Source: ClinicalTrials.gov
Cache Date: September 14, 2005

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December 5, 2009


Page Updated: June 1, 2005
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