Device Based Therapy in Hypertension Trial (DEBuT-HT)

CVRx

Status

Completed

Conditions

Hypertension

Treatments

Device: Rheos Baroreflex Hypertension Therapy System

Study type

Interventional

Funder types

Industry

Identifiers

NCT00710190

360004-001

Details and patient eligibility

About

The purpose of this study is to demonstrate the safety and efficacy of the Rheos Baroreflex Hypertension Therapy System in patients with refractory hypertension.

Full description

The DEBuT-HT trial will investigate the safety and efficacy of Rheos Baroreflex Hypertension Therapy(TM) in patients with refractory hypertension despite full pharmacologic therapy. Enrolled patients will be carefully assessed prior to receiving a permanently implanted Rheos System. Once the system is implanted, these patients will be followed closely for 1 month to establish baseline information. The Rheos System will be programmed "ON" at the 1 month follow-up and incrementally increased at 2 and 3-month follow-up evaluations. An assessment of safety and efficacy will be made at the 4-month follow-up. Enrolled patients will be followed annually thereafter.

Enrollment

46 patients

Sex

All

Ages

21+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Be at least 21 years of age.
Have been assessed to have bilateral carotid bifurcations located at or below C3 - C4.
Have blood pressure greater than or equal to 160 mmHg systolic and/or greater than or equal to 90 mmHg diastolic despite at least two months of full therapy with at least three (3) anti-hypertensive medications, of which at least one (1) must be a diuretic.
Must be certified by the investigator as compliant to taking full doses of medications.
Have signed an approved informed consent form for participation in this study.

Exclusion criteria

Have been diagnosed with:
- Baroreflex failure or significant orthostatic hypotension
- Cardiac brady arrhythmias or chronic atrial fibrillation
Have carotid atherosclerosis determined by ultrasound or angiographic evaluation with a stenosis of greater than 50%.
Have prior surgery or radiation in either carotid sinus region
Currently have implanted electrical medical devices such as cardiac pacing, defibrillation or neurologic stimulation systems.
Are pregnant or contemplating pregnancy during the 4-month follow-up period.
Are on dialysis
Have hypertension secondary to a treatable cause
Have clinically significant cardiac valvular disease
Are unable to comply with protocol requirements.
Are unlikely to survive the protocol follow-up period
Are enrolled in another concurrent clinical trial