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Effect at 6 Months of Renal Denervation in Chronic Heart Failure d'Insuffisance Cardiaque (DENRENIC)

Primary Purpose

Chronic Heart Failure

Status
Unknown status
Phase
Phase 1
Locations
France
Study Type
Interventional
Intervention
EnligHTN™ Renal Denervation System
Sponsored by
Institute Arnault Tzanck, France
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Heart Failure focused on measuring Cardio-Renal Syndrome, Chronic Heart Failure, Renal Denervation, Sympathetic activation, Heart Failure, Cardiovascular Diseases, Heart Diseases

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Stable chronic heart failure
  • NYHA III-IV
  • LV EF <35 assessed by ultrasound
  • EGFR> 45ml / min / 1.73m2
  • Optimal therapeutic treatment
  • IMC : 17-24

Exclusion Criteria:

  • significant renovascular abnormalities such as renal artery stenosis> 30%.
  • renal angioplasty history, renal denervation, stent placement
  • hemodynamically significant valvular heart disease
  • an active systemic infection.
  • renal artery of <4 mm.
  • coagulation abnormalities.
  • kidney transplant or is waiting for a kidney transplant.
  • life expectancy of less than 12 months (seatle score).
  • femoral-iliac atherosclerotic

Sites / Locations

  • Clinique Plein Ciel

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Renal Denervation

Arm Description

patients with chronique heart failure will undergo EnligHTN™ Renal Denervation System as a complementary treatment of their therapy

Outcomes

Primary Outcome Measures

Significant improvement of the 6 minutes walk test
The primary efficacy end point is the assessment at 6 months post renal denervation of the improvement in symptomatology as BNP level or VO2 max or pharmacological therapy from baseline

Secondary Outcome Measures

Incidence of adverse events
Assessment of renovascular safety as measured by new renal artery stenosis or aneurysm at the site of ablation Renal function change based on eGFR
Quality of life evaluated by EQ-5D. 1

Full Information

First Posted
June 8, 2015
Last Updated
October 18, 2016
Sponsor
Institute Arnault Tzanck, France
Collaborators
Abbott Medical Devices
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1. Study Identification

Unique Protocol Identification Number
NCT02471729
Brief Title
Effect at 6 Months of Renal Denervation in Chronic Heart Failure d'Insuffisance Cardiaque
Acronym
DENRENIC
Official Title
Evaluation à Six Mois du système de dénervation rénale Chez Les Patients Atteints d'Insuffisance Cardiaque
Study Type
Interventional

2. Study Status

Record Verification Date
October 2016
Overall Recruitment Status
Unknown status
Study Start Date
January 2017 (undefined)
Primary Completion Date
September 2017 (Anticipated)
Study Completion Date
January 2018 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Institute Arnault Tzanck, France
Collaborators
Abbott Medical Devices

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Management of chronic heart failure (CHF) is a major public health problem. It is associated with high mortality, frequent hospitalization and represents a large cost to the health care system. Both pharmacological and non-pharmacological intervention haven't shown to be effective in reducing morbidity and mortality of these patients when able to modulate the activity of neuro-hormonal systems among them the sympathetic nervous system. Recent data have emphasized the potential role of sympathetic renal denervation in patient with hypertension. CHF per se but even more CHF associated with comorbity lead to significant increase level of sympathetic tone. This is largely induced by autonomic dysfunction such as chemo or baroflex abnormalities. These patients usually suffer from conditions which do not allow upgrading and adapting drugs to their sympathetic condition. Hence CHF patient with chronic kidney disease, anemia or both have markedly high sympathetic activity and cannot be exposed to higher level of RAS Blockers or beta blocker due to their renal dysfunction, they thus remain with an elevated sympathetic activity worsening symptoms and prognosis. Chronic heart failure affects around 100 million people worldwild imposing a significant burden on health care system throughout the world. Even though symptoms are improved by heart failure therapy, they remain significantly disabling for many patients. Chronic over activation of the sympathetic nervous system is a major component of heart failure and involves efferent and afferent pathways between brain and many organs. A new therapy directly targeting nerve traffic-renal artery denervation- has been shown to be effective in drug resistant hypertension, with an average drop in blood pressure of 33/12 mm hg. The cardiologists team of the private hospital Arnault Tzanck is willing therefore to conduct a study in 12 patients with chronic systolic heart failure undergoing bilateral renal denervation with an intensive protocol of observation and assessment compring a 3 day hospital stay post procedure 3 and 6 months of regular outpatient follow-up.
Detailed Description
Renal denervation is a new interventional cardiology technique that involves using a catheter and a femoral artery, inserting an RF probe that will destroy the nerve fibers in contact with the wall of the renal artery with a very small electric current. The method utilizes the energy emitted by a miniaturized device positioned at the end of a catheter. This catheter is positioned in the arteries going to the kidneys. Sympathetic overactivation, is reduced by renal denervation in drug-resistant hypertension. Several studies conducted in patients without heart failure showed that renal denervation reduces left ventricular hypertrophy beyond its only effect on blood pressure. Chronic over activation of the sympathetic nervous system is a major component of heart failure and involves efferent and afferent pathways between brain and many organs. The purpose of this Clinical investigation is to evaluate the safety and performance of the EnligHTN™ Renal Denervation System in the treatment of patients with chronique heart failure. All patients will be on stable maximal tolerated pharmacological therapy for HFC prior to denervation. After the procedure all patients will be monitored as inpatients for 3 days so that hemodynamic disturbances could be identified. Baseline measurements, including BNP, echo Doppler VO2 and six minutes walk test will be repeated before discharge from hospital. After discharge patients will be followed up weekly for 4 weeks and then after 3 and 6 months. At the end of the study, bnp, echo Doppler Vo2 and six minutes walk test will be repeated, they also will be asked to categorize themselves as feeling worse, the same, or better in comparison to their preprocedural state.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Heart Failure
Keywords
Cardio-Renal Syndrome, Chronic Heart Failure, Renal Denervation, Sympathetic activation, Heart Failure, Cardiovascular Diseases, Heart Diseases

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
12 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Renal Denervation
Arm Type
Experimental
Arm Description
patients with chronique heart failure will undergo EnligHTN™ Renal Denervation System as a complementary treatment of their therapy
Intervention Type
Device
Intervention Name(s)
EnligHTN™ Renal Denervation System
Other Intervention Name(s)
EnligHTN™ Renal Artery Ablation Catheter, EnligHTN™ RF Generator, EnligHTN™ Guiding Catheter
Intervention Description
The renal nerve ablation will be performed according to the EnligHTN™ Renal Denervation System Instructions for Use. This system has the CE mark and is marketed in Europe and manufactured in France. The ablation catheter is indicated for use in renal denervation procedures for the treatment of hypertension.
Primary Outcome Measure Information:
Title
Significant improvement of the 6 minutes walk test
Description
The primary efficacy end point is the assessment at 6 months post renal denervation of the improvement in symptomatology as BNP level or VO2 max or pharmacological therapy from baseline
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Incidence of adverse events
Description
Assessment of renovascular safety as measured by new renal artery stenosis or aneurysm at the site of ablation Renal function change based on eGFR
Time Frame
5 months
Title
Quality of life evaluated by EQ-5D. 1
Time Frame
before intervention and after 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: Stable chronic heart failure NYHA III-IV LV EF <35 assessed by ultrasound EGFR> 45ml / min / 1.73m2 Optimal therapeutic treatment IMC : 17-24 Exclusion Criteria: significant renovascular abnormalities such as renal artery stenosis> 30%. renal angioplasty history, renal denervation, stent placement hemodynamically significant valvular heart disease an active systemic infection. renal artery of <4 mm. coagulation abnormalities. kidney transplant or is waiting for a kidney transplant. life expectancy of less than 12 months (seatle score). femoral-iliac atherosclerotic
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jean Louis LLORET, MD
Phone
33 (0)4.97.16.65.17
Email
jl.lloret@tzanck.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jean Louis LLORET, MD
Organizational Affiliation
Private hospital Mougins Arnault Tzanck
Official's Role
Principal Investigator
Facility Information:
Facility Name
Clinique Plein Ciel
City
Mougins
State/Province
Alpes Maritimes
ZIP/Postal Code
06254
Country
France
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jean Louis LLORET, MD

12. IPD Sharing Statement

Plan to Share IPD
No

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Effect at 6 Months of Renal Denervation in Chronic Heart Failure d'Insuffisance Cardiaque

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