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NCT04727840

Potassium Binder in CKD Patients (With Hyperkalemia) (DiPo Trial)

Status unknown Phase 1 Last updated 1 February 2021
What this trial tests

Phase 1 trial testing Sodium Zirconium Cyclosilicate Oral Product in Chronic Kidney Diseases in 20 participants. Status unknown.

Timeline
15 March 2021
Primary endpoint
15 January 2022
15 January 2022

Quick facts

Lead sponsorBrigham and Women's Hospital
PhasePhase 1
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment20
Start date15 March 2021
Primary completion15 January 2022
Estimated completion15 January 2022
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Brigham and Women's Hospital

Who can join

Adults 18 to 80, any sex, with Chronic Kidney Diseases or Hyperkalemia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study hypothesizes that the administration of Sodium zirconium cyclosilicate in CKD patients with hyperkalemia while avoiding dietary potassium restriction will normalize their serum potassium levels. Additionally, we aim to assess the effects of a high potassium diet on renal function, endothelial function, acidosis, systemic inflammatory status and gut microbiota.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Chronic Kidney Diseases

Currently open trials in the same condition.

Other Brigham and Women's Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04727840.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing