SYMPLICITY HTN-3 Renal Denervation in Patients With Uncontrolled Hypertension
Trial ID or NCT#
Status
Purpose
The Symplicity HTN-3 study is a, multi-center, prospective, single-blind, randomized, controlled study of the safety and effectiveness of renal denervation in subjects with uncontrolled hypertension. Bilateral renal denervation will be performed using the Symplicity Catheter - a percutaneous system that delivers radiofrequency (RF)energy through the luminal surface of the renal artery.
Official Title
Renal Denervation in Patients With Uncontrolled Hypertension (SYMPLICITY HTN-3)
Eligibility Criteria
- * Individual is ≥ 18 and ≤ 80 years old at time of randomization.* Individual is receiving a stable medication regimen including full tolerated doses of 3 or more anti-hypertensive medications of different classes, of which one must be a diuretic (with no changes for a minimum of 2 weeks prior to screening) that is expected to be maintained without changes for at least 6 months.* Individual has an office systolic blood pressure (SBP) of ≥ 160 mmHg based on an average of 3 blood pressure readings measured at both an initial screening visit and a confirmatory screening visit
- * Individual has an estimated glomerular filtration rate (eGFR) of \< 45 mL/min/1.73 m2* Individual has an Ambulatory Blood Pressure Monitoring (ABPM) 24 hour average SBP \< 135 mmHg* Individual has type 1 diabetes mellitus* Individual requires chronic oxygen support or mechanical ventilation (e.g., tracheostomy, CPAP, BiPAP) other than nocturnal respiratory support for sleep apnea.* Individual has primary pulmonary hypertension.* Individual is pregnant, nursing or planning to be pregnant.
Contact us to find out if this trial is right for you.
Contact
Maria Perlas
650-723-2094
View on ClinicalTrials.gov