Potassium pills may slow kidney decline in CKD patients
NCT ID NCT03253172
First seen Jun 27, 2026 · Last updated Aug 11, 2026 · Updated 2 times
Summary
This study tests whether taking potassium supplements can slow down kidney function loss in people with moderate-to-severe chronic kidney disease (CKD) and high blood pressure. About 532 adults with CKD stage 3b or 4 will receive potassium or a placebo. The goal is to see if potassium can protect the kidneys and lower blood pressure.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 532 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jul 2017
- Expected to finish
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Oct 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * CKD 3b or 4 (45 - 15 ml/min/1.73 m2) * Δ eGFR (as estimated by the CKD-EPI equation) \> 2 ml/min/1.73 m2/year (in preceding ≥ 1 year with at least 3 measurements) * Hypertension (defined as office blood pressure \> 140/90 mmHg or use of anti-hypertensive medication) Exclusion Criteria: * Hyperkalemia (serum potassium \> 5.5 mmol/l) at study visit V0 * Medical reasons to continue dual RAAS-blockade, mineralocorticoid receptor blockers, potassium-sparing diuretics, or oral potassium binders. * Patients with previous history of ventricular cardiac arrhythmia * Patients with a life expectancy \< 6 months * Expected initiation of renal replacement therapy \< 2 years * Incapacitated subjects * Women who are pregnant, breastfeeding or consider pregnancy in the coming 2 years.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Academic Medical Center Amsterdam
Amsterdam, Netherlands
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Erasmus MC
Rotterdam, Netherlands
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Leiden University Medical Center
Leiden, Netherlands
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University Medical Center Groningen
Groningen, Netherlands
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