Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT07399587 · ClinicalTrials.gov registry record · Phase 2

Optimizing HFrEF Patients Using BaroStim and CardioMems

A Phase 2 study of Heart Failure NYHA Class III, sponsored by Northwell Health.

Recruiting
Registry status
Phase 2
Development phase
15
Enrollment target
1
Study location

NCT07399587 is a Phase 2 study of Heart Failure NYHA Class III that is actively recruiting participants, run by Northwell Health. The registered enrollment target is 15 participants, below the 844-participant average among 9 other Heart Failure NYHA Class III trials with a reported enrollment target (98% lower). The trial reports 1 study location across 1 state.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT07399587, a Phase 2 study of Heart Failure NYHA Class III, is actively recruiting participants, sponsored by Northwell Health.

RECRUITING
Registry status
Phase 2
Development phase
15 participants
Enrollment target
1
Study location

Study Summary

The goal of this study is to utilize CardioMems (measurement of pulmonary artery diastolic pressure) to assess BaroStim. At the time of CardioMems insertion, patients will be screened for candidacy to receive a BaroStim device. Patients will be followed for 3 months after the CardioMems insertion before undergoing insertion of a Barostim. Patients who have undergone a CardioMems, will be eligible for enrollment after 3 months of medication management and optimization. Patients will be followed for 1 year after insertion of Barostim.

Interventions

  • DEVICE BaroStim

Study Locations (1)

New York

  • Peconic Bay Medical Center - Riverhead

Trial Details

FieldValue
Enrollment Target 15 participants
Start Date 2025-01-17
Est. Completion 2029-12-31
Phase Phase 2

Sponsor

Northwell Health

370 total trials

What the Registry Record Tells You About NCT07399587

The ClinicalTrials.gov registry entry for NCT07399587 describes a study currently listed as recruiting, categorized as Phase 2. The registered enrollment target is 15 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 844-participant average among 9 other Heart Failure NYHA Class III trials with a reported enrollment target (98% lower). The listed sponsor is Northwell Health, which has 370 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Heart Failure NYHA Class III appearing as the primary indexed condition, and to 1 intervention - of which BaroStim is the first listed.

NCT07399587 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.

Frequently Asked Questions

What is clinical trial NCT07399587 about?

NCT07399587 is a clinical study titled "Optimizing HFrEF Patients Using BaroStim and CardioMems". The goal of this study is to utilize CardioMems (measurement of pulmonary artery diastolic pressure) to assess BaroStim. At the time of CardioMems insertion, patients will be screened for candidacy to receive a BaroStim device. Patients will be followed for 3 months after the CardioMems insertion be...

What is the current status of trial NCT07399587?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 15 participants. The study started on 2025-01-17. Estimated completion is 2029-12-31.

What conditions does trial NCT07399587 study?

This clinical trial studies the following conditions: Heart Failure NYHA Class III.

What interventions are being tested in trial NCT07399587?

The interventions under investigation include: BaroStim (DEVICE).

Who is sponsoring clinical trial NCT07399587?

This trial is sponsored by Northwell Health, which has 370 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07399587 being conducted?

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

Similar trials for Heart Failure NYHA Class III

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

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

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, or report a data error.