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Clinical Trial Summary

NephroNet proposes to examine whether combining Spironolactone with maximal RAAS blockade will further reduce urinary protein at one year and whether prolonged therapy (24 months) is able to slow the decline in GFR. Because of combination MRA and RAAS therapy significantly increases the risk for clinically significant hyperkalemia, we also plan to determine whether the addition of Patiromer to these patients facilitates the use of combination therapy and allows a larger proportion of diabetic patients the potential benefit of combination therapy on renal function.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03502031
Study type Interventional
Source NephroNet, Inc.
Contact James A Tumlin, MD
Phone 770-490-9203
Email jamestumlinmdnephronet@gmail.com
Status Recruiting
Phase Phase 4
Start date October 1, 2018
Completion date October 1, 2024

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