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Device
Renal Denervation for High Blood Pressure
N/A
Recruiting
Led By David Kandzari, MD
Research Sponsored by Medtronic Vascular
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Individual is diagnosed with hypertension and has a baseline office systolic blood pressure ≥140 mmHg
Diagnosed with hypertension and has a baseline office systolic blood pressure ≥140 mmHg
Must not have
Lacks appropriate renal artery anatomy
Has undergone prior renal denervation
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 6 months
Awards & highlights
No Placebo-Only Group
Summary
This trial is studying the safety and effectiveness of a device called the Symplicity Spyral system, which helps lower blood pressure by calming overactive nerves in the kidneys. It includes patients who have already received this treatment. The Symplicity Spyral system is part of a series of treatments, with earlier versions showing significant blood pressure reductions in patients with resistant hypertension.
Who is the study for?
This trial is for individuals with high blood pressure (systolic ≥140 mmHg) who may also have diabetes, kidney disease, or cardiovascular issues. It's not suitable for those with severe kidney impairment (eGFR <30), pregnant women, or anyone lacking the right renal artery anatomy.
What is being tested?
The study tests the Symplicity Spyral system's safety and effectiveness in lowering blood pressure through renal denervation—a procedure that disrupts nerve signals to the kidneys.
What are the potential side effects?
While specific side effects are not listed here, renal denervation procedures can potentially cause nerve damage, bleeding, infection, or negative reactions related to catheter-based treatments.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I have high blood pressure with a reading of 140 mmHg or higher.
Select...
I have high blood pressure with a reading of 140 mmHg or higher.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
My kidney arteries are not suitable for the procedure.
Select...
I have had a procedure to decrease nerve activity in my kidneys.
Select...
I need oxygen or a ventilator daily, not just for sleep apnea at night.
Select...
I have experienced dizziness due to a sudden drop in blood pressure when standing up.
Select...
I have high blood pressure in the lungs.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 6 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
The Primary endpoint of office Systolic Blood Pressure (SBP) change at 6 months.
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: Main Cohort: Renal DenervationExperimental Treatment1 Intervention
Renal angiography and Renal Denervation (Symplicity Spyral™ multi-electrode renal denervation system)
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Renal Denervation (Symplicity Spyral™)
2020
N/A
~130
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for Chronic Kidney Disease (CKD) focus on managing hypertension, a critical factor in disease progression. ACE inhibitors and ARBs reduce the effects of angiotensin II, leading to blood vessel dilation, lower blood pressure, and decreased intraglomerular pressure, which helps protect kidney function.
Renal denervation, a newer treatment, disrupts renal nerves to reduce sympathetic nerve activity and lower blood pressure. This is particularly important for CKD patients with resistant hypertension, as it offers an alternative method to control blood pressure and potentially slow the progression of the disease.
[A Chinese Nephrology and Dialysis Unit in the eyes of a western nephrologist].Rapidly deteriorating renal function with membranoproliferative glomerulonephritis Type 1 associated with hepatitis C treated successfully with steroids and antiviral therapy: a case report and review of literature.
[A Chinese Nephrology and Dialysis Unit in the eyes of a western nephrologist].Rapidly deteriorating renal function with membranoproliferative glomerulonephritis Type 1 associated with hepatitis C treated successfully with steroids and antiviral therapy: a case report and review of literature.
Find a Location
Who is running the clinical trial?
Medtronic VascularLead Sponsor
66 Previous Clinical Trials
56,067 Total Patients Enrolled
David Kandzari, MDPrincipal InvestigatorPiedmont Heart Institute
17 Previous Clinical Trials
6,943 Total Patients Enrolled
Felix Mahfoud, MDPrincipal InvestigatorSaarland University Hospital
7 Previous Clinical Trials
2,990 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- My kidney arteries are not suitable for the procedure.You have a medical condition that makes it hard to get an accurate blood pressure reading.I need oxygen or a ventilator daily, not just for sleep apnea at night.I have high blood pressure with a reading of 140 mmHg or higher.Your kidney function, measured by eGFR, is very low.I have high blood pressure in the lungs.I have had a procedure to decrease nerve activity in my kidneys.I have high blood pressure with a reading of 140 mmHg or higher.I have experienced dizziness due to a sudden drop in blood pressure when standing up.
Research Study Groups:
This trial has the following groups:- Group 1: Main Cohort: Renal Denervation
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Chronic Kidney Disease Patient Testimony for trial: Trial Name: NCT05198674 — N/A
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