SYMPLICITY HTN-3 Renal Denervation in Patients With Uncontrolled Hypertension

Medtronic

Status: Completed

Conditions: Uncontrolled Hypertension

Treatments: Diagnostic Test: Renal angiogram; Device: Renal denervation (Symplicity Catheter System)

Study type: Interventional

Funder types: Industry

Identifiers

NCT01418261

IP125

Details and patient eligibility

About

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.

Full description

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.

Enrollment: 535 patients

Sex: All

Ages: 18 to 80 years old

Volunteers: No Healthy Volunteers

Inclusion 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

Exclusion criteria

• 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.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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535 participants in 2 patient groups

Renal Denervation

Experimental group

Description:

Subjects are treated with the renal denervation procedure after randomization and maintained baseline anti-hypertensive medications

Treatment:

Device: Renal denervation (Symplicity Catheter System)

Diagnostic Test: Renal angiogram

Control group

Sham Comparator group

Description:

Subjects go through renal angiogram and Subjects maintained baseline anti-hypertensive medications

Treatment:

Diagnostic Test: Renal angiogram