Effect of Renal Sympathetic Denervation on Resistant Hypertension and Cardiovascular Hemodynamic in Comparison to Intensive Medical Therapy Utilizing Impedance Cardiography (OsloRDN)
Hypertension, Resistant to Conventional Therapy

About this trial
This is an interventional treatment trial for Hypertension, Resistant to Conventional Therapy focused on measuring Renal sympathetic denervation, Impedance cardiography
Eligibility Criteria
Inclusion Criteria:
- Average SBP >140mmHg, measured per guidelines
- 24 hour average ABPM daytime SBP >135mm/Hg
- On stable medication regimen of full tolerated doses of 3 or more antihypertensive meds, with one being a diuretic
- No changes for a minimum of 2 weeks prior to screening
- No planned medication changes for 6 months
- Age 18-80 years
- At minimum, 3 antihypertensive medications must meet one or more of the following full dose criteria:
- Highest labeled dose according to medication's labeling
- Highest usual dose per clinical guidelines-JNC-7
- Highest tolerated dose
- Highest appropriate dose for the patient per the PI's clinical judgment
Exclusion Criteria:
- Hemodynamically or anatomically significant renal artery abnormalities or stenosis >50% or prior renal artery intervention
- eGFR < 45 mL/min/1.73m2 (MDRD formula)
- Albumin/creatinine ratio > 50 mg/mmol
- Type 1 diabetes mellitus
- Known alcohol or drug abuse
- Symptomatic orthostatic hypotension in past year
- Stenotic valvular heart disease for which BP reduction would be hazardous
- MI, unstable angina, or CVA in the prior 6 months
- Known primary pulmonary HTN
- Known pheochromocytoma, Cushing's disease, coarctation of the aorta, hyperthyroidism or hyperparathyroidism
- Known primary hyperaldosteronism not adequately treated.
Sites / Locations
- Oslo University Hospital
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
group Co
group RDN
group Co receives intensive medical therapy utilizing integrated hemodynamic management calculated by impedance cardiography of "The HOTMAN® System"
For patients who will be randomly assigned to undergo renal denervation by "The SymplicityTM Renal Denervation System", the femoral artery will be accessed with the standard endovascular technique and the catheter will be advanced into the renal artery and connected to a radiofrequency generator. As in Symplicity HTN 1 and 2 trials, four-to-six discrete, low-power radiofrequency ablations lasting up to 2 min each and of 8 watts or less to obtain up to four-six ablations separated both longitudinally and rotationally within each renal artery. During ablation, the catheter system monitored tip temperature and impedance, altering radiofrequency energy delivery in response to a predetermined algorithm.