Effects of Spironolactone Combination Therapy on Proteinuria, Kidney Function, and Blood Pressure

Last updated: August 27, 2012
Sponsor: Tehran University of Medical Sciences
Overall Status: Completed

Phase

2

Condition

Nephropathy

Diabetes Mellitus, Type 2

Diabetes Mellitus Types I And Ii

Treatment

N/A

Clinical Study ID

NCT01667614
90-2-27-16-10
  • Ages 40-80
  • All Genders

Study Summary

The detrimental effects of aldostrone are not adequately arrested by the use of angiotensin converting enzyme (ACE), angiotensin II receptor blocker (ARB) or a combination of both. Recent evidence has provided robust evidence that aldostrone escape plays an important role in this regard. It is believed that aldostrone escape occurs quite commonly with reports indicating prevalence rates as high as 22% with ARBs and 40% with ACE inhibitors. In a trial of patients with diabetes and hypertension it was shown that treatment of aldostrone escape with spironolactone 25 mg daily for three months significantly reduces proteinuria. A number of other trials have similarly observed that addition of spironolactone to an ACE inhibitor based regimen provides additional benefits on proteinuria reduction, blood pressure control, and prevention of glomerular filtration rate (GFR) decline. Most of the available trials in this regard are of short duration (e.g. three months), and have added spironolactone to an ACE or ACE+ARB based regimen (the so-called triple blockade). Currently, evidence evaluating efficacy of a combined ARB+spironolactone regimen compared with conventional double RAS blockade (i.e. ACE+ARB) is lacking. Hence, this randomized open label trial was initiated to determine the effects of addition of spironolactone 25 mg daily to losartan over a period of 18 months.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • type 2 diabetes patients with diabetic nephropathy in the range of micro- ormacroalbuminuria

  • treatment with combination of enalapril and losartan for more than one year

Exclusion

Exclusion Criteria:

  • history of non-adherence to prescribed medication assessed by the prescribingphysician

  • baseline potassium > 5.5 meq/L

  • chronic kidney disease stages 4 or 5

  • history or evidence of non-diabetic kidney disease

Study Design

Total Participants: 136
Study Start date:
May 01, 2010
Estimated Completion Date:
July 31, 2012

Connect with a study center

  • Tehran University of Medical Sciences, Vali-asr hospital, Endocrinology and Metabolism Research Center

    Tehran, 13145-784
    Iran, Islamic Republic of

    Site Not Available

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