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Hyperkalemia

Spironolactone With Patiromer in the Treatment of Resistant Hypertension in Chronic Kidney Disease
NCT03071263 | PHASE 2 | INTERVENTIONAL

The purpose of this study is to determine if patiromer treatment in chronic kidney disease (CKD) subjects receiving spironolactone for the treatment of resistant hypertension will result in more persistent use of spironolactone through prevention of hyperkalemia and lead to improved blood pressure control compared with treatment with spironolactone alone (placebo).

Trial Information
40 Sites
295 Participants
Recruiting
18 Years to 64 Years

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Investigator Site
Hollywood,Florida,United States,33021
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Miami Lakes,Florida,United States,33014
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Chicago,Illinois,United States,60611
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Sofia,Bulgaria,1612
Investiagor Site
Zagreb,Croatia,10000
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Zagreb,Croatia,10000
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Zagreb,Croatia,10000
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Zagreb,Croatia,10000
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Tbilisi,Georgia,0102
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Tbilisi,Georgia,0112
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Tbilisi,Georgia,0144
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Tbilisi,Georgia,0159
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Tbilisi,Georgia,0159
Investigator Site
Tbilisi,Georgia,0159
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Tbilisi,Georgia,0159
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Tbilisi,Georgia,0159
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Tbilisi,Georgia,0159
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Tbilisi,Georgia,0159
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Tbilisi,Georgia,0159
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Tbilisi,Georgia,0186
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Gottingen,Germany,37075
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Balatonfured,Hungary,H-8230
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Budapest,Hungary,H-1097
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Debrecen,Hungary,4032
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Hatvan,Hungary,H-3000
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Kistarcsa,Hungary,H-2143
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Miskolc,Hungary,H-3529
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Miskolc,Hungary,H-3530
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Mosonmagyarovar,Hungary,H-9200
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Johannesburg,South Africa
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Khar'kov,Ukraine,61006
Investiagor Site
Kharkiv,Ukraine,61002
Investigator Site
Kharkiv,Ukraine,61039
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Kharkiv,Ukraine,61103
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Kiev,Ukraine,03680
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Kiev,Ukraine,04114
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Zaporizhzhia,Ukraine,69001
Investigator Site
Zaporizhzhia,Ukraine,69118
Investigator Site
Leicester,United Kingdom,LE54QF
Investigator Site
London,United Kingdom,Se59RS

Study Eligibility Criteria

Additional Studies

Additional studies can be found at ClinicalTrials.gov