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Renal Denervation in Patients With Heart Failure and Severe Left Ventricular Dysfunction.

Primary Purpose

Heart Failure

Status
Unknown status
Phase
Not Applicable
Locations
Czech Republic
Study Type
Interventional
Intervention
Catheterised renal denervation
Sponsored by
University Hospital Olomouc
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Heart Failure focused on measuring Heart failure, Renal denervation

Eligibility Criteria

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

Inclusion Criteria:

  • Patients over 18 years of age with chronic heart failure, ischemic and non-ischemic etiology.
  • NYHA (New York Heart Association) class II-IV.
  • LVEF (Left Ventricular Ejection Fraction) ≤ 35%.
  • Patients treated with maximum tolerated doses of standard pharmacotherapy for heart failure, who were stable for at least four weeks without acute decompensated heart failure.
  • Prior to enrollment, patients must give informed consent.

Exclusion Criteria:

  • Patients with history of acute coronary syndrome or stroke within the last 6 months.
  • Significant valvular defects and/or planned cardiac surgery.
  • Systolic blood pressure <110 mmHg.
  • Advanced renal insufficiency (estimated GFR (Glomerular Filtration Rate) according to MDRD <30 ml/min/1.73 square meters).
  • Unsuitable anatomy of renal arteries (presence of significant renal stenosis, renal artery narrower than 4 mm).
  • Patients who underwent renal angioplasty or stent placement into the renal artery in the past.
  • Severe coagulation disorders.
  • Pregnancy or lactation.
  • Refusal of the patient.
  • Other diseases limiting prognosis of the patient to less than 2 years.
  • Other reasons which in the opinion of the attending physician would preclude the individual from participating in the study.

Sites / Locations

  • University Hospital, OlomoucRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Standard medical therapy

Renal denervation + standard medical therapy

Arm Description

Patients in this arm will undergo catheterised renal denervation in addition to having optimization of medical therapy for heart failure.

Outcomes

Primary Outcome Measures

Change in serum NT-proBNP at 6 months and 1 year from baseline in both groups.
The level of NT-proBNP (N-terminal prohormone of Brain Natriuretic Peptide) is a reliable indicator of the severity of heart failure. Lowering levels will indicate improvement in the heart function.

Secondary Outcome Measures

Reduction in the number of hospitalizations and/or deaths due to cardiovascular causes.

Full Information

First Posted
May 25, 2013
Last Updated
June 3, 2013
Sponsor
University Hospital Olomouc
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1. Study Identification

Unique Protocol Identification Number
NCT01870310
Brief Title
Renal Denervation in Patients With Heart Failure and Severe Left Ventricular Dysfunction.
Official Title
Long Term Study on the Possible Beneficial Effects of Catheterised Renal Denervation in Patients With Heart Failure and Left Ventricular Systolic Dysfunction Who Are Already on Standard Medical Therapy.
Study Type
Interventional

2. Study Status

Record Verification Date
June 2013
Overall Recruitment Status
Unknown status
Study Start Date
June 2012 (undefined)
Primary Completion Date
September 2013 (Anticipated)
Study Completion Date
June 2016 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Hospital Olomouc

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
It is a randomized prospective controlled study evaluating the effect of transcatheter renal denervation on the clinical status of patients with chronic heart failure and its safety procedures. The working hypothesis of the study is that by performing transcatheter renal denervation in patients with chronic heart failure and severe left ventricular systolic dysfunction there will a resultant reduction in the renal sympathetic activation which in turn will reduce the number of hospitalizations and deaths from heart failure.
Detailed Description
Chronic heart failure in the European countries occurs in 2-3% of the population with a significant increase in the higher age groups (1). Improved treatment of acute conditions (especially myocardial infarction) has resulted in more patients entering into the category of chronic heart failure. Chronic heart failure has a poor prognosis. Diagnosis and treatment are challenging both medically and economically. Half of the patients with systolic heart failure die within 4 years and more than 50% of patients with severe heart failure (NYHA functional class of IV) die within one year (1). The current treatments for heart failure are not only aimed at influencing the symptoms, but also preventing the progression of heart failure to reduce mortality. Heart failure leads to the activation of compensatory mechanisms designed to restore adequate cardiac output. These mechanisms are initially beneficial, but their long-term activation leads to further progression of the pathological process and deterioration of cardiac function. One of the basic pathophysiological processes in heart failure is excessive activation of the sympathetic nervous system. This causes increased levels of circulating catecholamines which is proportional to the severity of the disease that is patients with the highest levels of norepinephrine have the worst prognosis. Beta-blocker therapy which is designed to inhibit activity of sympathetic nervous system causes milder symptoms of heart failure in patients by modifying disturbed hemodynamics and ultimately the clinical status. In recent years, the therapeutic efficacy of beta-blockers in chronic heart failure has been verified in a number of controlled clinical trials (2-5). These studies have confirmed that long-term treatment with beta-blocker therapy alleviates the symptoms of heart failure, improves the clinical condition of the patients and reduces mortality like ACE inhibitors. High activity of renal sympathetic nerves in patients with chronic heart failure is an early predictor of increased mortality (6). The main pathophysiological basis of this finding is probably excessive sodium retention due to direct activation of sympathetic fibers innervating renal tubules (7). Recent experimental work on animals have shown that surgical renal denervation inhibits an increase in renal vascular resistance, prevents a decrease in renal blood flow (8), and also prevents changes in expression of angiotensin receptors in the kidney (8). Surgical sympathectomy began to be used for the treatment of severe and malignant hypertension more than 50 years ago. But this was a rather complicated procedure, which was accompanied by a number of adverse effects (orthostatic hypotension and tachycardia, shortness of breath, bowel and sexual disorders]. Moreover it required a long hospitalization of 2-4 weeks and then required a recovery period of 1-2 months. However this intervention led to a rapid decrease in pressure and a higher survival rate after surgery in a large observational study(9). In recent years a method has been developed in which destruction of renal sympathetic nerves that are present in the adventitia of renal arterial walls is done by catheterization (10). This procedure uses a catheter with a radiofrequency ablator at its tip (Symplicity, Ardian / Medtronic, USA), which is introduced through the femoral artery and then progressively introduced into the renal arteries. A randomized study has demonstrated that this procedure has a high degree of safety for the patients and a high rate of efficacy as well. In patients with resistant hypertension treated with transcatheter renal denervation there was a significant drop in blood pressure of 33/11 mmHg (p < 0.0001) that occurred after 6 months compared to a control group receiving unmodified pharmacological treatment (11).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Failure
Keywords
Heart failure, Renal denervation

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Standard medical therapy
Arm Type
No Intervention
Arm Title
Renal denervation + standard medical therapy
Arm Type
Experimental
Arm Description
Patients in this arm will undergo catheterised renal denervation in addition to having optimization of medical therapy for heart failure.
Intervention Type
Procedure
Intervention Name(s)
Catheterised renal denervation
Other Intervention Name(s)
Symplicity, Ardian / Medtronic, USA
Primary Outcome Measure Information:
Title
Change in serum NT-proBNP at 6 months and 1 year from baseline in both groups.
Description
The level of NT-proBNP (N-terminal prohormone of Brain Natriuretic Peptide) is a reliable indicator of the severity of heart failure. Lowering levels will indicate improvement in the heart function.
Time Frame
6 months and 1 year
Secondary Outcome Measure Information:
Title
Reduction in the number of hospitalizations and/or deaths due to cardiovascular causes.
Time Frame
1 year to 4 years
Other Pre-specified Outcome Measures:
Title
Significant Renal impairment and symptomatic hypotension.
Description
Increase in serum creatinine of 2 times the baseline or decrease in estimated glomerular filtration according to MDRD (Modification of Diet in Renal Disease) by more than 50% from baseline will be used to assess renal function.
Time Frame
6 months to 1 year

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: Patients over 18 years of age with chronic heart failure, ischemic and non-ischemic etiology. NYHA (New York Heart Association) class II-IV. LVEF (Left Ventricular Ejection Fraction) ≤ 35%. Patients treated with maximum tolerated doses of standard pharmacotherapy for heart failure, who were stable for at least four weeks without acute decompensated heart failure. Prior to enrollment, patients must give informed consent. Exclusion Criteria: Patients with history of acute coronary syndrome or stroke within the last 6 months. Significant valvular defects and/or planned cardiac surgery. Systolic blood pressure <110 mmHg. Advanced renal insufficiency (estimated GFR (Glomerular Filtration Rate) according to MDRD <30 ml/min/1.73 square meters). Unsuitable anatomy of renal arteries (presence of significant renal stenosis, renal artery narrower than 4 mm). Patients who underwent renal angioplasty or stent placement into the renal artery in the past. Severe coagulation disorders. Pregnancy or lactation. Refusal of the patient. Other diseases limiting prognosis of the patient to less than 2 years. Other reasons which in the opinion of the attending physician would preclude the individual from participating in the study.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Dagmar Strnkova, Mgr.
Phone
+420 588 443 716
Email
dagmarstrnkova@seznam.cz
First Name & Middle Initial & Last Name or Official Title & Degree
Albert Louis, MUDr.
Phone
+420 588 443 238
Email
albertlouis3@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Miloš Táborský, doc., MUDr., CSc., FESC, MBA
Organizational Affiliation
Head of Department of First Clinic of Internal Medicine - Cardiology, University Hospital, Olomouc.
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital, Olomouc
City
Olomouc
ZIP/Postal Code
775 20
Country
Czech Republic
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Miloš Táborský, doc., MUDr., CSc., FESC, MBA
Phone
+420 588 443 201
Email
milos.taborsky@fnol.cz
First Name & Middle Initial & Last Name & Degree
Albert Louis, MUDr.
Phone
+420 588 443 238
Email
albertlouis3@gmail.com
First Name & Middle Initial & Last Name & Degree
Miloš Táborský, doc., MUDr., CSc., FESC, MBA
First Name & Middle Initial & Last Name & Degree
Albert Louis, MUDr.

12. IPD Sharing Statement

Citations:
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18799522
Citation
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Renal Denervation in Patients With Heart Failure and Severe Left Ventricular Dysfunction.

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