Spironolactone in Diabetic Nephropathy
Primary Purpose
Diabetic Nephropathy
Status
Completed
Phase
Phase 4
Locations
Denmark
Study Type
Interventional
Intervention
Spironolactone
Sponsored by
About this trial
This is an interventional treatment trial for Diabetic Nephropathy focused on measuring Diabetic nephropathy, Spironolactone, Aldosterone antagonism, Renoprotection
Eligibility Criteria
Inclusion Criteria: Diabetes Mellitus Diabetic Nephropathy Glomerular filtration rate > 30 ml/min/1.73 m2 Blood pressure > 130/80 mm Hg Exclusion Criteria: Child bearing potential Plasma-potassium >4.5 mmol/l Breastfeeding Abuse of alcohol or drugs Non-diabetic kidney disease
Sites / Locations
- Steno Diabetes Center
Outcomes
Primary Outcome Measures
Changes in albuminuria
Changes in blood pressure
Secondary Outcome Measures
Changes in glomerular filtration rate
Full Information
NCT ID
NCT00317954
First Posted
April 21, 2006
Last Updated
April 21, 2006
Sponsor
Steno Diabetes Center Copenhagen
1. Study Identification
Unique Protocol Identification Number
NCT00317954
Brief Title
Spironolactone in Diabetic Nephropathy
Official Title
Spironolactone in Diabetic Nephropathy
Study Type
Interventional
2. Study Status
Record Verification Date
August 2005
Overall Recruitment Status
Completed
Study Start Date
September 2003 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
July 2005 (undefined)
3. Sponsor/Collaborators
Name of the Sponsor
Steno Diabetes Center Copenhagen
4. Oversight
5. Study Description
Brief Summary
The aim of the study was to evaluate the renoprotective effect (i.e. albuminuria- and bloodpressure lowering effect) of spironolactone 25 mg o.d. in type 1 and type 2 diabetic patients with albuminuria despite recommended antihypertensive treatment.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetic Nephropathy
Keywords
Diabetic nephropathy, Spironolactone, Aldosterone antagonism, Renoprotection
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Crossover Assignment
Masking
Double
Allocation
Randomized
Enrollment
48 (false)
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
Spironolactone
Primary Outcome Measure Information:
Title
Changes in albuminuria
Title
Changes in blood pressure
Secondary Outcome Measure Information:
Title
Changes in glomerular filtration rate
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Diabetes Mellitus
Diabetic Nephropathy
Glomerular filtration rate > 30 ml/min/1.73 m2
Blood pressure > 130/80 mm Hg
Exclusion Criteria:
Child bearing potential
Plasma-potassium >4.5 mmol/l
Breastfeeding
Abuse of alcohol or drugs
Non-diabetic kidney disease
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hans-Henrik Parving, MD,DMSc,Prof
Organizational Affiliation
Steno Diabetes Center Copenhagen
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Katrine J Schjoedt, MD
Organizational Affiliation
Steno Diabetes Center Copenhagen
Official's Role
Principal Investigator
Facility Information:
Facility Name
Steno Diabetes Center
City
Gentofte
ZIP/Postal Code
2820
Country
Denmark
12. IPD Sharing Statement
Citations:
PubMed Identifier
16316360
Citation
Schjoedt KJ, Rossing K, Juhl TR, Boomsma F, Rossing P, Tarnow L, Parving HH. Beneficial impact of spironolactone in diabetic nephropathy. Kidney Int. 2005 Dec;68(6):2829-36. doi: 10.1111/j.1523-1755.2005.00756.x.
Results Reference
result
PubMed Identifier
16123474
Citation
Rossing K, Schjoedt KJ, Smidt UM, Boomsma F, Parving HH. Beneficial effects of adding spironolactone to recommended antihypertensive treatment in diabetic nephropathy: a randomized, double-masked, cross-over study. Diabetes Care. 2005 Sep;28(9):2106-12. doi: 10.2337/diacare.28.9.2106.
Results Reference
result
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Spironolactone in Diabetic Nephropathy
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