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

NCT07335510 · ClinicalTrials.gov registry record · NA

Impact of Barostimulation on Hemodynamics in Adults With Heart Failure

A NA study, sponsored by Columbia University.

Recruiting
Registry status
NA
Development phase
58
Enrollment target

NCT07335510: Recruiting NA study, sponsored by Columbia University.

NCT07335510 is a NA study that is actively recruiting participants, run by Columbia University. The registered enrollment target is 58 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT07335510, a NA study, is actively recruiting participants, sponsored by Columbia University.

RECRUITING
Registry status
NA
Development phase
58 participants
Enrollment target

Study Summary

This study evaluates the effects of the implantation and adjustment of the CVRx Barostim device in adult patients with heart failure with reduced ejection fraction who are receiving maximally tolerated doses of guideline directed medical and device therapies. The study aims to assess how therapy using this device affects heart function, symptoms, and exercise capacity, with particular focus on how the device affects blood flow and heart pressures during exercise. Information from this study may help inform patient selection and device management in patients with heart failure.

Primary Outcome

Exercise pulmonary capillary wedge pressure (PCWP) will be measured at peak exercise at approximately six months post-Barostim titration and compared with peak exercise PCWP measured during the pre-implantation phase. Change from baseline will be calculated.

Interventions

  • DEVICE Baroreflex Activation Therapy

Trial Details

FieldValue
Enrollment Target 58 participants
Start Date 2026-03-30
Est. Completion 2028-03
Phase NA
Columbia University

958 total trials

What NCT07335510 shows while recruiting

NCT07335510 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 58 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).

The record links to 0 conditions, and to 1 intervention - of which Baroreflex Activation Therapy is the first listed.

NCT07335510 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT07335510 about?

NCT07335510 is a clinical study titled "Impact of Barostimulation on Hemodynamics in Adults With Heart Failure". This study evaluates the effects of the implantation and adjustment of the CVRx Barostim device in adult patients with heart failure with reduced ejection fraction who are receiving maximally tolerated doses of guideline directed medical and device therapies. The study aims to assess how therapy usi...

What is the current status of trial NCT07335510?

This trial is currently recruiting. It is a NA study. The enrollment target is 58 participants. The study started on 2026-03-30. Estimated completion is 2028-03.

What interventions are being tested in trial NCT07335510?

The interventions under investigation include: Baroreflex Activation Therapy (DEVICE).

Who is sponsoring clinical trial NCT07335510?

This trial is sponsored by Columbia University, which has 958 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT07335510's enrollment target sits among peer trials

58 1256th of 2000 higher than 740 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT03587844 · 58 participants · Phase 2

    Dosing of Brentuximab Vedotin for Mycosis Fungoides, Sezary Syndrome Patients

  • NCT03630991 · 58 participants · Phase 1

    Edetate Calcium Disodium or Succimer in Treating Patients With Acute Myeloid Leukemia or Myelodysplastic Syndrome Undergoing Chemotherapy

  • NCT03949855 · 58 participants · Phase 2

    Belimumab With Rituximab for Primary Membranous Nephropathy

  • NCT04069273 · 58 participants · Phase 2

    Novel SEQUEnced Immunotherapy With Anti-angiogenesis and Chemotherapy in Advanced gastroesophageaL Adenocarcinoma

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT07335510, the US trial registry maintained by the National Library of Medicine. NCT07335510 (small enrollment · none site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.