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BAROSTIM THERAPY™ In Resistant Hypertension

Recruitingn/aAges any - anyAllCVRx, Inc.
NCT02880631 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

The purpose of this registry (NCT02880631) is to evaluate the effect of BAROSTIM THERAPY with the BAROSTIM NEO System in the commercial setting in subjects recently implanted under the CE-Marked indication for resistant hypertension.

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📋 Eligibility rules (as published)
Inclusion Criteria: * Has signed an EC approved informed consent form * Has been implanted with the BAROSTIM NEO system in the past 30 days * Systolic blood pressure greater than or equal to 140 mmHg, and * Resistance to maximally tolerated therapy with a diuretic and two other anti-hypertension medications Exclusion Criteria: * Bilateral carotid bifurcations located above the level of the mandible * Baroreflex failure or autonomic neuropathy * Uncontrolled, symptomatic cardiac bradyarrhythmias * Carotid atherosclerosis that is determined by ultrasound or angiographic evaluation to be greater than 50% * Ulcerative plaques in the carotid artery as determined by ultrasound or angiographic evaluation
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What it tests

  • BAROSTIM NEO™ System
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Where

26 sites
Charité Benjamin Franklin
Berlin, Germany
Charité Campus Virchow
Berlin, Germany
Immanuel Klinikum Bernau Herzzentrum Brandenburg
Bernau, Germany
Cloppenburg Katholische Kliniken Münsterland
Cloppenburg, Germany
Universitätsklinikum Köln Herzzentrum
Cologne, Germany
Lippe Klinikum
Detmold, Germany
Herzzentrum Dresden
Dresden, Germany
Krankenhaus Erding
Erding, Germany

…and 18 more on ClinicalTrials.gov.

🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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