NCT Number: NCT00240019
Maximizing the Benefit of Renin-Angiotensin Blocking Drugs in Diabetic Renal Disease.
The angiotensin converting enzyme inhibitor drugs are now standard therapy for patients with diabetic nephropathy. The hypothesis of this study is that adding a diuretic agent (furosemide) will decrease the urine protein, which is a sign of disease, more than an angiotensin converting enzyme inhibitor alone.
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Notify MeKey information
Conditions
Age range
18 year–80 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Not applicable
Primary location
Kaiser Permanente of Northern California, Santa Clara and San Jose, Santa Clara, California, United States
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
proteinuria greater than 1 gram/day serum creatinine < 2.6 for men, < 2.0 for women
Exclusion criteria
blood pressure which cannot be controlled without a diuretic renal diseases other than diabetic nephropathy other disease which would alter renal function during 6 months
Treatment and study plan
Primary outcomes
-
The amount of protein in the urine after 8 weeks of treatment.
Secondary outcomes
-
The estimated glomerular filtration rate after 8 weeks of treatment.
Sponsors and collaborators
Lead sponsor
Stanford University
Other
Collaborators
- National Institutes of Health (NIH)
Registry information
Official study title
Maximizing the Benefit of RAS Blockade in Diabetic Nephropathy
Important dates
- Study start
- 2003
- Study completion
- 2006
- First posted
- Oct 17, 2005
- Registry last updated
- Oct 17, 2006
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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