Not provided
Not provided
Not provided
Not provided
Manufacturer updated device technology.
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Class |
|---|---|
| Medtronic | INDUSTRY |
| Mars Excellence in Clinical Innovation and Technology Evaluation | OTHER |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
The purpose of this study is to evaluate the clinical and economic impact of implementation of renal denervation with the Symplicityâ„¢ Catheter System for treatment-resistant hypertension in Ontario, Canada.
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.
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Early renal denervation | Experimental | Renal denervation takes place immediately after patient is randomized. |
|
| Delayed renal denervation | Other | Renal denervation takes place 6 months after the patient is randomized. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Renal denervation device | Device |
|
|
| Measure | Description | Time Frame |
|---|---|---|
| Average systolic 24-hour ambulatory blood pressure | 6 months |
| Measure | Description | Time Frame |
|---|---|---|
| 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 | |
| Average daytime and average night-time systolic ambulatory blood pressure |
Not provided
Inclusion Criteria:
Exclusion Criteria:
Secondary causes of hypertension:
Type 1 diabetes mellitus
Pregnancy
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Affiliation | Role |
|---|---|---|
| Harindra C. Wijeysundera, MD | Sunnybrook Research Institute | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Sunnybrook Research Institute | Toronto | Ontario | M4N 3M5 | Canada | ||
| St. Michael's Hospital |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| 6 months |
| Variability of 24-hour ambulatory systolic blood pressure | 6 months |
| Average office blood pressure using an approved, automated office blood pressure device | 6 months |
| Hypertensive medication complexity index (MRCI) | 6 months |
| Number of hypertensive medications | 6 months |
| Peri-procedural mean cost per patient in Canadian dollars | 12 months |
| Generic quality of life (EQ-5D) | 6 months |
| Body Mass Index (BMI) | 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 |
| Vascular complications (dissection, pseudoaneurysm, AV fistula) | 6 months |
| Evidence of renal artery stenosis compared to pre-procedure (determined by renal imaging, CT or MRA) for early intervention group | 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 |
| Microalbumin to creatinine ratio (MACR) from random urine sample (% change from baseline) | 6 months |
| 24-hour urine sodium (% change from baseline) | 6 months |
| Toronto |
| Ontario |
| M5B 1W8 |
| Canada |