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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00870402
Other study ID # SA08I20032
Secondary ID
Status Recruiting
Phase Phase 4
First received March 25, 2009
Last updated March 25, 2009
Start date March 2009
Est. completion date March 2010

Study information

Verified date March 2009
Source Universidad Los Andes, Chile
Contact Francisco G Espinoza, MD
Phone 56 - 2 -91380529
Email fespinoz@mi.cl
Is FDA regulated No
Health authority Chile: Comisión Nacional de Investigación Científica y Tecnológica
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine whether spironolactone are effective in the reduction of albuminuria and diastolic disfunction of subjects with diabetic nephropathy.


Recruitment information / eligibility

Status Recruiting
Enrollment 160
Est. completion date March 2010
Est. primary completion date December 2009
Accepts healthy volunteers No
Gender Both
Age group 30 Years to 70 Years
Eligibility Inclusion Criteria:

- Diabetic subjects with maximum ten years after diagnostic

- Diabetic nephropathy with albuminuria

- Normal renal function

- Diastolic disfunction

- Taking a IECA or ARA drug family previously

Exclusion Criteria:

- Diabetics subjects with macroangiopathy

- Acute coronary syndrome in the three months before

- Hyperkalemia > 5.5 mEq/L

- Pregnancy

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment


Intervention

Drug:
Spironolactone
25 mg per day for 9 months
Placebo
Placebo 1 tablet per day for nine months

Locations

Country Name City State
Chile University of Los Andes Santiago

Sponsors (1)

Lead Sponsor Collaborator
Universidad Los Andes, Chile

Country where clinical trial is conducted

Chile, 

References & Publications (1)

Kozie DW, Hassul M, Kimm J. Effect of tympanic membrane perforations on air caloric response in monkeys. Trans Sect Otolaryngol Am Acad Ophthalmol Otolaryngol. 1976 Mar-Apr;82(2):203-9. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Reduction of albuminuria 9 months Yes
Secondary Reduction of diastolic disfunction 9 months Yes
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