Heart Failure Clinical Trial

Cardionomic STOP-ADHF Study

Summary

STOP-ADHF Study: An evaluation of the safety and performance of the Cardionomic Cardiac Pulmonary Nerve Stimulation (CPNS) system in patients with acute decompensated heart failure.

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Full Description

The STOP-ADHF is a prospective, two-arm, multi-center study to evaluate the safety and performance of the CPNS System in patients with acute decompensated heart failure (ADHF).

The CPNS System is a neuromodulation system, intended to provide acute (≤5 days) endovascular stimulation of the cardiac autonomic nerves in the right pulmonary artery. The system consists of a temporary neuromodulation stimulator catheter and a stimulator.

Approximately 90 patients will be enrolled in the study and will be followed up through 6-months post-discharge from the hospital. Patients enrolled in the treatment group will receive CPNS therapy and followed closely in an intensive care unit setting. Patients enrolled in the control arm in will receive standard treatment for their heart failure.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Admitted to hospital with a principal diagnosis of ADHF
BMI adjusted BNP ≥ 500 pg/mL or NT-proBNP ≥ 2000 pg/mL
LVEF ≤ 50%
At least one sign or symptom of fluid overload despite the administration of IV furosemide (or equivalent) (at least 40 mg or equivalent)

Exclusion Criteria:

Received a high dose inotrope or Levosimendan during current hospitalization or treatment with a low dose inotriope within 24 hours before enrollment
Requires mechanical support
Cardiogenic shock or impending cardiogenic shock
Systolic blood pressure < 80mmHg or > 140mmHg
Symptomatic hypotension
eGFR < 25 mL/min/1.732

Study is for people with:

Heart Failure

Estimated Enrollment:

90

Study ID:

NCT04814134

Recruitment Status:

Recruiting

Sponsor:

Cardionomic Inc.

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There are 10 Locations for this study

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St. Vincent Hospital
Indianapolis Indiana, 46260, United States
Summa Health
Akron Ohio, 44309, United States
The Christ Hospital
Cincinnati Ohio, 45219, United States
University Hospitals
Cleveland Ohio, 44106, United States
The Ohio State University
Columbus Ohio, 43210, United States
Oklahoma Heart Hospital South
Oklahoma City Oklahoma, 73135, United States
TriStar Centennial Medical Center
Nashville Tennessee, 37203, United States
Medical City Fort Worth
Fort Worth Texas, 76104, United States
Baylor College of Medicine
Houston Texas, 77030, United States
OLV Ziekenhuis
Aalst , , Belgium
AZ Sint-Jan Brugge
Bruges , , Belgium
Antwerp University Hospital
Edegem , , Belgium
University Medical Center Groningen
Groningen , , Netherlands
St. Antonius Ziekenhuis
Nieuwegein , 3435C, Netherlands
Punta Pacifica
Panama City , , Panama

How clear is this clinincal trial information?

Study is for people with:

Heart Failure

Estimated Enrollment:

90

Study ID:

NCT04814134

Recruitment Status:

Recruiting

Sponsor:


Cardionomic Inc.

How clear is this clinincal trial information?

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