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Terminated Phase 4 Interventional

Patiromer Utility as an Adjunct Treatment in Patients Needing Urgent Hyperkalemia Management

ClinicalTrials.gov ID: NCT04443608

Public ClinicalTrials.gov record NCT04443608. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 21, 2026, 5:04 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel Group Phase 4 Study of the Efficacy & Safety of Patiromer for Oral Suspension in Combination With Standard of Care Treatment in ED Patients With Hyperkalemia

Study identification

NCT ID
NCT04443608
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 4
Lead sponsor
Comprehensive Research Associates
Industry
Enrollment
115 participants

Conditions and interventions

Conditions

Interventions

  • Patiromer Powder for Oral Suspension [Veltassa] Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 7, 2020
Primary completion
Mar 8, 2023
Completion
Jun 2, 2023
Last update posted
Aug 30, 2023

2020 – 2023

United States locations

U.S. sites
19
U.S. states
13
U.S. cities
16
Facility City State ZIP Site status
Stanford University School of Medicine Stanford California 94305
Yale University New Haven Connecticut 06519
Christiana Care Newark Delaware 19718
George Washington University Washington D.C. District of Columbia 20037
Baystate Medical Center Springfield Massachusetts 01199
Wayne State University Detroit Michigan 48201
Henry Ford Hospital Detroit Michigan 48202
Hennepin Healthcare Research Institute Minneapolis Minnesota 55415
University of Mississippi Medical Center Jackson Mississippi 39216
Washington University of St Louis St Louis Missouri 63110
Mt Sinai. Icahn School of Medicine New York New York 10029
Maimonides Medical Center New York New York 11219
Stony Brook University Hospital Stony Brook New York 11794
Wake Forest University Health Sciences Winston-Salem North Carolina 27157
University of Cincinnati Cincinnati Ohio 45219
Ohio State University. Wexner Medical Center Columbus Ohio 43210
JPS Health Network Fort Worth Texas 76104
Baylor College of Medicine Houston Texas 77030
UT Memorial Hermann Hospital Houston Texas 77030

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04443608, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 30, 2023 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04443608 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →