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Clinical Trials/NCT01895140
NCT01895140
Terminated
Not Applicable

A Pragmatic Randomized Clinical Evaluation of Renal Denervation for Treatment Resistant Hypertension

Dr. Harindra Wijeysundera2 sites in 1 country8 target enrollmentOctober 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Treatment-Resistant Hypertension
Sponsor
Dr. Harindra Wijeysundera
Enrollment
8
Locations
2
Primary Endpoint
Average systolic 24-hour ambulatory blood pressure
Status
Terminated
Last Updated
11 years ago

Overview

Brief Summary

The purpose of this study is to evaluate the clinical and economic impact of implementation of renal denervation with the Symplicity™ Catheter System for treatment-resistant hypertension in Ontario, Canada.

Detailed Description

This is a pragmatic randomized trial of renal nerve denervation for treatment resistant hypertension. This is part of a ministry sponsored MaRS-EXCITE program, to conduct early market health technology assessment, in order to determine appropriateness for provincial funding. We will assess the effectiveness, safety, economic attractiveness and feasibility of implementation of renal nerve denervation for treatment resistant hypertension. This will involve a new model of care which will include a multi-disciplinary team approach to these patients. Treatment resistant hypertension is defined as patients with uncontrolled hypertension despite being on optimal doses of 3 or more anti-hypertensive medications. Patients will be randomized to either standard treatment or renal nerve denervation and followed for 6 months to determine impact on blood pressure.

Registry
clinicaltrials.gov
Start Date
October 2013
End Date
October 2014
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Dr. Harindra Wijeysundera
Responsible Party
Sponsor Investigator
Principal Investigator

Dr. Harindra Wijeysundera

Interventional Cardiologist

Sunnybrook Health Sciences Centre

Eligibility Criteria

Inclusion Criteria

  • Ontario residents
  • Aged 18 and over
  • Diagnosis of treatment-resistant hypertension after assessment and optimization by a hypertension specialist following recommended evaluation and diagnosis as outlined by the American Heart Association
  • Office systolic blood pressure ≥ 160 mmHg (≥ 150 mmHg for patients with type II diabetes mellitus) prior to optimization by a hypertension specialist
  • Baseline average systolic 24 hour ambulatory blood pressure of ≥ 135 mmHg after optimization and prior to randomization
  • Prescribed 3 or more antihypertensive medications of different classes, both prior to optimization and at randomization, one of which must be a diuretic (a medication can be counted more than once if it acts on different receptors)
  • Suitable renal artery anatomy based on CT/MRI/renal angiography imaging: both renal arteries \> 20 mm in length and \> 4 mm in diameter without significant fibromuscular disease or renal artery stenosis (\>50%)

Exclusion Criteria

  • Secondary causes of hypertension:
  • Primary aldosteronism (secondary to adrenal adenoma)
  • Chronic kidney disease: creatinine clearance or eGFR \< 45 ml/min/1.73m² (measured on 24 hour urine preferably or MDRD)
  • Pheochromocytoma
  • Cushing's syndrome
  • Aortic coarctation (differential in brachial or femoral pulses, systolic bruit)
  • Type 1 diabetes mellitus
  • Pregnancy

Outcomes

Primary Outcomes

Average systolic 24-hour ambulatory blood pressure

Time Frame: 6 months

Secondary Outcomes

  • Average office blood pressure using an approved, automated office blood pressure device(6 months)
  • Peri-procedural mean cost per patient in Canadian dollars(12 months)
  • Hypertensive medication complexity index (MRCI)(6 months)
  • Body Mass Index (BMI)(6 months)
  • Vascular complications (dissection, pseudoaneurysm, AV fistula)(6 months)
  • Average daytime and average night-time systolic ambulatory blood pressure(6 months)
  • Number of hypertensive medications(6 months)
  • Composite cardiovascular endpoints (fatal & non-fatal MI, new onset heart failure, stroke, beginning dialysis, hospitalization for cardiovascular/renal reasons, increase in hypertension medications)(6 months)
  • 24-hour urine sodium (% change from baseline)(6 months)
  • Evidence of renal artery stenosis compared to pre-procedure (determined by renal imaging, CT or MRA) for early intervention group(6 months)
  • Proportion of patients achieving target systolic blood pressure (on average 24-hour ambulatory blood pressure of <130 mmHg) on the same or fewer medications at the time of randomization(6 months)
  • Variability of 24-hour ambulatory systolic blood pressure(6 months)
  • Generic quality of life (EQ-5D)(6 months)
  • 24-hour urine sodium(6 months)
  • Acute periprocedural renal injury(72 hours post procedure)
  • Creatinine clearance measured on 24-hour urine (% change from baseline & indexed to Body Surface Area)(6 months)
  • Microalbumin to creatinine ratio (MACR) from random urine sample (% change from baseline)(6 months)

Study Sites (2)

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