Renal Denervation in Hypertrophic Cardiomyopathy (SNYPER-PS)
Primary Purpose
Hypertrophic Cardiomyopathy
Status
Recruiting
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
"Symplicity Spyral" multi-electrode renal denervation catheter and "Symplicity G3" generator (Renal Denervation System)
Sponsored by
About this trial
This is an interventional treatment trial for Hypertrophic Cardiomyopathy focused on measuring renal denervation
Eligibility Criteria
Inclusion Criteria:
- Sarcomeric HCM (absence of metabolic, syndromic or neurological diseases with increased left ventricular thickness) confirmed by genetic study (pathogenic or probably pathogenic variant identified in a sarcomeric gene).
- NYHA Class II-IV despite optimal therapy for the last 30 days.
- Left ventricular septum > 16 mm.
- Age between 18 and 80 years.
- Not candidate to septal reduction therapy or valve surgery.
Exclusion Criteria:
- Non sarcomeric causes of increased left ventricular thickness.
- Left ventricular systolic disfunction (EF < 50%) or dilatation (indexed left ventricular end diastolic volume [LVEDV] > 75 ml/m2 for men and > 62 ml/m2 for women).
- Blood pressure < 100/50 mmHg.
- Severe functional impairment due to concomitant diseases.
- Renal glomerular filtration < 30 ml/min/m2 (Cockcroft-Gault´s formula).
- Hospitalization for heart failure, stroke or acute coronary syndrome (ACS) in the last 30 days.
- Heart failure requiring inotropic drugs or intravenous diuretics over the last 30 days, or in the waiting list for heart transplantation.
- Unfavorable renal artery anatomy (significant stenosis, diameter < 2mm, length < 4mm)
- Women on pregnancy, lactation or fertile age without contraception.
- Parkinson´s disease or Lewy body dementia.
- Life expectancy less than one year
- Unwilling to sign informed consent or to undergo study procedure and visits.
- Participation in other clinical trial over the last 30 days.
Sites / Locations
- Hospital Universitario 12 de OctubreRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
renal denervation
Arm Description
Renal denervation shall be performed by echo-guided catheterization of the femoral artery, and subsequent cannulation of the renal arteries with a guide catheter. A renal denervation catheter shall be advanced through the guide catheter to the distal portion of the artery. The procedures shall be aimed to deliver as many radiofrequency applications as possible, 0.5 cm apart, intended duration of 60 sec, to all four quadrants of the renal arteries and main branch vessels with > 3 mm diameter.
Outcomes
Primary Outcome Measures
Cardiac sympathetic nerve activity (123I-MIBG washout rate)
123I-MIBG washout rate measured by scintigraphy
Secondary Outcome Measures
Functional status
New York Heart Association (NYHA) class. From I to IV (higher scores mean a worse outcome)
Left ventricular mass
Left ventricular mass assessed by echocardiography (Devereux´s formula, septal and posterior wall thickness)
Diastolic function
E / A ratio, deceleration time, E' septal and lateral velocity, E/E´ septal ratio, propagation velocity assessed by echocardiography
Subaortic gradient (left ventricular outflow tract obstruction [LVOT])
Baseline peak LVOT gradient, peak LVOT gradient during Valsalva in millimeters of mercury
Number of ventricular tachycardia episodes
Non-sustained ventricular tachycardias episodes recorded by a cardiac electronic implantable device (pacemaker or defibrillator, if previously implanted)
Heart rate variability
Number of atrial premature complexes and number of non-sustained atrial tachycardias recorded by 24-hour Holter
Maximum oxygen consumption
Maximum oxygen consumption assessed by ergospirometer
Blood pressure
Mean, daily and nocturnal systolic and diastolic blood pressure assessed by 24-hour ambulatory monitoring of blood pressure (AMBP)
NT-Pro-BNP
Serum NT-Pro-BNP levels
Kansas City Cardiomyopathy Questionnaire (KCCQ) score
Self-administered health-related quality of life questionnaire composed by 23 items, which provides a score range from 0 to 100.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT05577208
Brief Title
Renal Denervation in Hypertrophic Cardiomyopathy
Acronym
SNYPER-PS
Official Title
Cardiac Sympathetic Neuromodulation by Renal Denervation in Hypertrophic Cardiomyopathy (SNYPER Pilot Study)
Study Type
Interventional
2. Study Status
Record Verification Date
November 2022
Overall Recruitment Status
Recruiting
Study Start Date
November 26, 2022 (Actual)
Primary Completion Date
June 30, 2024 (Anticipated)
Study Completion Date
December 31, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Adolfo Fontenla
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Hypertrophic cardiomyopathy (HCM) is the most common inherited monogenic heart disease. There is an abnormal increase in myocardial mass in this disorder that leads to a state of cardiac sympathetic hypertonia, which is involved in disease progression, development of arrhythmias and heart failure. Cardiac sympathetic hyperactivity may constitute a new therapeutic target in HCM patients who persist symptomatic despite conventional treatment. The hypothesis of this project is that renal denervation (a minimally invasive percutaneous interventional therapy with proven efficacy in resistant arterial hypertension) reduces cardiac sympathetic activity in HCM. The SNYPER pilot study is a non-randomized clinical trial with medical devices (proof of concept), in which a renal denervation procedure will be performed in 20 patients with genetically confirmed sarcomeric HCM, severe left ventricular hypertrophy and persistent symptoms. The impact of denervation in reducing the 123I-meta iodo benzyl guanidine (MIBG) washout rate quantified by isotopic tracing (planar imaging and SPECT) at 6 months is established as a primary efficacy objective, and the proportion of renal denervation-related complications as a safety objective. The most relevant secondary endpoints are the outcomes of renal denervation on left ventricular mass (echocardiogram), diastolic function, maximum oxygen consumption (ergospirometer), ventricular arrhythmia burden (Holter), blood pressure (ABPM), N-terminal (NT) Pro Brain Natriuretic Peptide (BNP) and quality of life (KCCQ questionnaire). The results of this study may open the development of a new, technically simple and easily accessible therapeutic line for the treatment of HCM.
Detailed Description
According to current literature, approximately two-thirds of patients with HCM have persistent symptoms despite conventional treatment. For this reason, novel nonpharmacological therapies such as cardiac resynchronization, endocardial catheter ablation of the interventricular septum or needle-based septal ablation have been proposed, however, none of them having been generalized up to date. Besides, these novel therapies cannot be applied in non-obstructive HCM. The abnormal activation of the sympathetic system represents a relevant mechanism in he pathophysiology of HCM, since it may have implications in the progression and prognosis of the disease. The modulation of the cardiac sympathetic tone by renal denervation could be developed as a new therapeutic target for patients with persistent symptoms despite conventional treatment.
The SNYPER pilot study is a prospective, single-center, single-arm, pilot study, evaluating renal denervation in patients with sarcomeric HCM and persistent symptoms despite optimal therapy, over a follow-up period of 6 months. It represents a proof of concept that will quantify the degree in which renal denervation modulates cardiac sympathetic activity in HCM, thus opening a new research line: a non-pharmacological, minimally invasive and safe treatment with potential positive impact on health and well-being of patients with HCM.
This is a non-commercial, investigator-driven clinical study funded through a public competitive call by Health Institute Carlos III, Spanish Ministry of Economy (PI21/00480).
The study is coordinated by the main investigator from "University Hospital 12 de Octubre" in Madrid. Several responsibilities are delegated to the Clinical Research Unit ("University Hospital 12 de Octubre", Madrid, Spain).
The study was planned according to the Good Clinical Practices. SNYPER Pilot Study has been approved by the Ethics Committee and Spanish Health Authorities. All participating patients must give written informed consent before any study procedure occur.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypertrophic Cardiomyopathy
Keywords
renal denervation
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
renal denervation
Arm Type
Experimental
Arm Description
Renal denervation shall be performed by echo-guided catheterization of the femoral artery, and subsequent cannulation of the renal arteries with a guide catheter. A renal denervation catheter shall be advanced through the guide catheter to the distal portion of the artery. The procedures shall be aimed to deliver as many radiofrequency applications as possible, 0.5 cm apart, intended duration of 60 sec, to all four quadrants of the renal arteries and main branch vessels with > 3 mm diameter.
Intervention Type
Device
Intervention Name(s)
"Symplicity Spyral" multi-electrode renal denervation catheter and "Symplicity G3" generator (Renal Denervation System)
Intervention Description
Minimally invasive percutaneous interventional therapy aimed to modulate the sympathetic nervous system through endovascular ablation of both renal arteries
Primary Outcome Measure Information:
Title
Cardiac sympathetic nerve activity (123I-MIBG washout rate)
Description
123I-MIBG washout rate measured by scintigraphy
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Functional status
Description
New York Heart Association (NYHA) class. From I to IV (higher scores mean a worse outcome)
Time Frame
6 months
Title
Left ventricular mass
Description
Left ventricular mass assessed by echocardiography (Devereux´s formula, septal and posterior wall thickness)
Time Frame
6 months
Title
Diastolic function
Description
E / A ratio, deceleration time, E' septal and lateral velocity, E/E´ septal ratio, propagation velocity assessed by echocardiography
Time Frame
6 months
Title
Subaortic gradient (left ventricular outflow tract obstruction [LVOT])
Description
Baseline peak LVOT gradient, peak LVOT gradient during Valsalva in millimeters of mercury
Time Frame
6 months
Title
Number of ventricular tachycardia episodes
Description
Non-sustained ventricular tachycardias episodes recorded by a cardiac electronic implantable device (pacemaker or defibrillator, if previously implanted)
Time Frame
6 months
Title
Heart rate variability
Description
Number of atrial premature complexes and number of non-sustained atrial tachycardias recorded by 24-hour Holter
Time Frame
6 months
Title
Maximum oxygen consumption
Description
Maximum oxygen consumption assessed by ergospirometer
Time Frame
6 months
Title
Blood pressure
Description
Mean, daily and nocturnal systolic and diastolic blood pressure assessed by 24-hour ambulatory monitoring of blood pressure (AMBP)
Time Frame
6 months
Title
NT-Pro-BNP
Description
Serum NT-Pro-BNP levels
Time Frame
6 months
Title
Kansas City Cardiomyopathy Questionnaire (KCCQ) score
Description
Self-administered health-related quality of life questionnaire composed by 23 items, which provides a score range from 0 to 100.
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Sarcomeric HCM (absence of metabolic, syndromic or neurological diseases with increased left ventricular thickness) confirmed by genetic study (pathogenic or probably pathogenic variant identified in a sarcomeric gene).
NYHA Class II-IV despite optimal therapy for the last 30 days.
Left ventricular septum > 16 mm.
Age between 18 and 80 years.
Not candidate to septal reduction therapy or valve surgery.
Exclusion Criteria:
Non sarcomeric causes of increased left ventricular thickness.
Left ventricular systolic disfunction (EF < 50%) or dilatation (indexed left ventricular end diastolic volume [LVEDV] > 75 ml/m2 for men and > 62 ml/m2 for women).
Blood pressure < 100/50 mmHg.
Severe functional impairment due to concomitant diseases.
Renal glomerular filtration < 30 ml/min/m2 (Cockcroft-Gault´s formula).
Hospitalization for heart failure, stroke or acute coronary syndrome (ACS) in the last 30 days.
Heart failure requiring inotropic drugs or intravenous diuretics over the last 30 days, or in the waiting list for heart transplantation.
Unfavorable renal artery anatomy (significant stenosis, diameter < 2mm, length < 4mm)
Women on pregnancy, lactation or fertile age without contraception.
Parkinson´s disease or Lewy body dementia.
Life expectancy less than one year
Unwilling to sign informed consent or to undergo study procedure and visits.
Participation in other clinical trial over the last 30 days.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Adolfo Fontenla, MD, PhD
Phone
+34699012607
Email
adolforamon.fontela@saludmadrid.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Adolfo Fontenla, MD, PhD
Organizational Affiliation
Hospital Universitario 12 de Octubre
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Adolfo Fontenla, MD, PhD
Organizational Affiliation
Hospital Universitario 12 de Octubre
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital Universitario 12 de Octubre
City
Madrid
ZIP/Postal Code
28015
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Adolfo Fontenla, MD, PhD
Email
adolforamon.fontela@saludmadrid.org
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
10 milliliters (mL) of total blood, 5mL of serum and 10mL of blood with a commercial formula for RNA preservation shall be collected and stored for future proteomic and genetic analysis.
IPD Sharing Time Frame
not defined
IPD Sharing Access Criteria
not defined
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Renal Denervation in Hypertrophic Cardiomyopathy
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