Clinical trial

Antiproteinuric Efficacy of Losartan Potassium in Patients With Non-Diabetic…

NCT00140985 · Organon and Co, Industry · Completed

Key facts

NCT number NCT00140985
Title Antiproteinuric Efficacy of Losartan Potassium in Patients With Non-Diabetic Proteinuric Renal Diseases (0954-213)
Official title A Randomized, Parallel, Double Blind Study of Losartan Versus Amlodipine in Patients With Mild to Moderate Hypertension and Chronic Nondiabetic Proteinuric Nephropathy: Evaluation of the Effect on Proteinuria and on the Plasmatic Levels of Growth Factors (TGFß and VEGF)
Lead sponsor Organon and Co, Industry
Status Completed
Phase Phase 4
Study type Interventional
Conditions Renal Disorder
Intervention type Drug
Interventions MK0954, losartan potassium/Duration of Treatment: 20 weeks, Comparator: amlodipine / Duration of Treatment: 20 weeks
Enrollment 97
Start date Feb 1, 2000
Primary completion Jan 1, 2002
Completion Jan 1, 2002
First posted Sep 1, 2005
Last update posted Feb 16, 2022

At a glance

  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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