Uncontrolled Hypertension Clinical Trial
Official title:
Renal Sympathetic Denervation for the Management of Chronic Hypertension
Despite the development of numerous drug therapies designed to treat hypertension, it
remains a considerable and poorly managed health, social and economic burden. For various
reasons, including the significant health care costs of treatment, there are estimates that
up to 65% of hypertensive patients have untreated and/or uncontrolled blood pressure (BP).
Aside from its impact on renal function, chronic hypertension significantly increases the
risk for stroke, coronary artery disease, heart failure, and vascular disease. It is
believed to be involved in the progression of cardiac arrhythmias. This link between
hypertension and cardiovascular health has been well described; as has their combined effect
on the aging and obesity-battling Western world.
The recently published results of the Symplicity HTN-2 trial (Renal sympathetic denervation
in patients with treatment resistant hypertension) establishing the therapeutic benefit of
catheter-based renal sympathetic denervation for hypertension, have enormous potential for
the management of a large and challenging patient population. The proposed, multicenter
trial will attempt to confirm and expand on this promising data by conducting a
double-blinded, placebo-controlled trial.
Patients may qualify to participate in this research study if their doctor has determined
that they have drug-resistant, chronic hypertension.
Overall participation in this research study should be about 13 months which includes about
1 month to start the study procedure and 12 months of follow-up after the study procedure.
Patients who qualify for the study and provide consent will undergo a renal angiogram in
order to assess suitability for catheter-based renal sympathetic denervation. A renal
angiogram is an x-ray study of the blood vessels in the kidney to evaluate for blockage, and
abnormalities that could be affecting the blood supply to the kidney. It is performed by
injecting contrast dye through a catheter (a tiny tube) into the blood vessels of the
kidney. The study doctor will assess whether the renal arteries are suitable to receive
catheter-based renal denervation.
Both groups will receive sedation or anesthesia prior to the beginning of the procedure.
The first group will undergo catheter-based sympathetic renal denervation. Renal Sympathetic
Denervation is a procedure that uses a catheter probe inserted into the renal (kidney)
artery that deactivates the nerves that are linked to high blood pressure.
The second group will only receive renal angiography without the delivery of ablative
energy.
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Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment
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