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NCT03781089 · ClinicalTrials.gov registry record · Phase 4

Patiromer Efficacy to Reduce Episodic Hyperkalemia in End Stage Renal Disease Patients

A Phase 4 study of End Stage Renal Disease and Hyperkalemia, sponsored by Duke University.

Completed
Registry status
Phase 4
Development phase
36
Enrollment target
1
Study location

NCT03781089 is a Phase 4 study of End Stage Renal Disease and Hyperkalemia that has completed, run by Duke University. The registered enrollment target is 36 participants, below the 833-participant average among 86 other End Stage Renal Disease trials with a reported enrollment target (96% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT03781089, a Phase 4 study of End Stage Renal Disease and Hyperkalemia, has completed, sponsored by Duke University.

COMPLETED
Registry status
Phase 4
Development phase
36 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to determine whether once-daily dosing of patiromer will reduce the frequency of hyperkalemic episodes in ESRD (end stage renal disease) study participants who receive conventional hemodialysis (HD). The study objective is to determine if patiromer administered orally once a day with breakfast or lunch will reduce episodes of hyperkalemia in ESRD study participants who receive thrice-weekly HD.

Interventions

  • DRUG Patiromer Oral Powder Product

Study Locations (1)

North Carolina

  • DaVita Dialysis Sites - Durham

Trial Details

FieldValue
Enrollment Target 36 participants
Start Date 2019-06-20
Est. Completion 2023-03-15
Phase Phase 4

Sponsor

Duke University

1,725 total trials

What the Registry Record Tells You About NCT03781089

The ClinicalTrials.gov registry entry for NCT03781089 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 36 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 833-participant average among 86 other End Stage Renal Disease trials with a reported enrollment target (96% lower). The listed sponsor is Duke University, which has 1,725 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with End Stage Renal Disease appearing as the primary indexed condition, and to 1 intervention - of which Patiromer Oral Powder Product is the first listed.

NCT03781089 reports 1 study location spanning 1 distinct geographic area - top geographies include North Carolina.

Frequently Asked Questions

What is clinical trial NCT03781089 about?

NCT03781089 is a clinical study titled "Patiromer Efficacy to Reduce Episodic Hyperkalemia in End Stage Renal Disease Patients". The purpose of this study is to determine whether once-daily dosing of patiromer will reduce the frequency of hyperkalemic episodes in ESRD (end stage renal disease) study participants who receive conventional hemodialysis (HD). The study objective is to determine if patiromer administered orally on...

What is the current status of trial NCT03781089?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 36 participants. The study started on 2019-06-20. Estimated completion is 2023-03-15.

What conditions does trial NCT03781089 study?

This clinical trial studies the following conditions: End Stage Renal Disease, Hyperkalemia.

What interventions are being tested in trial NCT03781089?

The interventions under investigation include: Patiromer Oral Powder Product (DRUG).

Who is sponsoring clinical trial NCT03781089?

This trial is sponsored by Duke University, which has 1,725 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03781089 being conducted?

This trial has 1 study location across North Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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