Cardiac Output Autonomic Stimulation Therapy for Heart Failure (COAST-HF) - Human NeuroCatheter S… (NCT02880683) | Clinical Trial Compass
CompletedNot Applicable
Cardiac Output Autonomic Stimulation Therapy for Heart Failure (COAST-HF) - Human NeuroCatheter Study
Paraguay16 participantsStarted 2015-10
Plain-language summary
A single-center feasibility study in patients undergoing cardiac catheterization, to investigate the acute hemodynamic effects of transvenous cardiac autonomic nerve stimulation.
Who can participate
Age range21 Years – 75 Years
SexALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Stable symptomatic heart failure - New York Heart Association Class II or III
* Normal Sinus Rhythm
Exclusion Criteria:
* Unable to gain arterial or venous access using standard percutaneous techniques
* New York Heart Association Class IV
* Patient taking amiodarone or other anti-arrhythmic therapy
* Patients with implanted pacemaker, ICD, or CRT device
* Patients who had CABG, PCI or enzyme-positive MI within prior month
* Patients with pre-existing carotid artery or cerebral disease
* Patients with hypertrophic obstructive cardiomyopathy or infiltrative cardiomyopathy (e.g. amyloidosis, sarcoidosis)
* Patients who have been hospitalized for heart failure and who required the use of heart failure IV therapy within 30 days before enrollment (measured from release)
* Patients with current or prior vagal nerve simulator
* Patients with renal failure
* Patients with hepatic failure
* Patients with narrow angle glaucoma
* Patients who are pregnant
* Patients with a life expectancy \< 12 months per physician judgment
* Patients with allergy to fentanyl, midazolam, propofol, eggs, egg products, soybeans, or soy products