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NCT04551222 · ClinicalTrials.gov registry record · Phase 2

The Re-Prosper HF Study

A Phase 2 study, sponsored by VA Office of Research and Development.

Completed
Registry status
Phase 2
Development phase
99
Enrollment target

NCT04551222: Completed Phase 2 study, sponsored by VA Office of Research and Development.

NCT04551222 is a Phase 2 study that has completed, run by VA Office of Research and Development. The registered enrollment target is 99 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04551222, a Phase 2 study, has completed, sponsored by VA Office of Research and Development.

COMPLETED
Registry status
Phase 2
Development phase
99 participants
Enrollment target

Study Summary

Heart failure with reduced ejection fraction (HFrEF) is a common cause for admission within the Veterans Affairs (VA) Health Care System. It is associated with severe impairment of physical and mental health status and carries a high risk of mortality. Even though significant progress has been made in understanding the disease process, currently, its management and treatment is limited. The investigators have discovered that a commonly used drug for the treatment of gout can be repurposed for the treatment of HFrEF. The objective of this study is the treatment of outpatient Veterans with HFrEF with probenecid to improve heart and health function. Specifically, the investigators are testing whether oral probenecid administered orally twice per day for 180 days improves heart function as measured via ultrasound of the heart (aim 1); improves exercise capacity (aim 2); and improves self-report heart failure specific health status as measured via questionnaires (aim 3).

Interventions

  • DRUG Placebo
  • DRUG probenecid

Trial Details

FieldValue
Enrollment Target 99 participants
Start Date 2021-06-09
Est. Completion 2025-12-31
Phase Phase 2

Sponsor

VA Office of Research and Development

1,668 total trials

What the Registry Record Tells You About NCT04551222

The ClinicalTrials.gov registry entry for NCT04551222 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 99 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is VA Office of Research and Development, which has 1,668 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT04551222 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT04551222 about?

NCT04551222 is a clinical study titled "The Re-Prosper HF Study". Heart failure with reduced ejection fraction (HFrEF) is a common cause for admission within the Veterans Affairs (VA) Health Care System. It is associated with severe impairment of physical and mental health status and carries a high risk of mortality. Even though significant progress has been made...

What is the current status of trial NCT04551222?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 99 participants. The study started on 2021-06-09. Estimated completion is 2025-12-31.

What interventions are being tested in trial NCT04551222?

The interventions under investigation include: Placebo (DRUG), probenecid (DRUG).

Who is sponsoring clinical trial NCT04551222?

This trial is sponsored by VA Office of Research and Development, which has 1,668 total clinical trials registered on ClinicalTrials.gov.

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

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, the data changelog, or report a data error.