Study of Renal Denervation in Patients With Heart Failure (PRESERVE)

Promotion of Renal Sodium Excretion by Renal Sympathetic Denervation in Congestive Heart Failure

Congestive heart failure is a common disorder in which the heart cannot pump enough blood to meet the needs of the rest of the body. Poor sodium handling by the kidneys is a damaging effect of heart failure, and it leads to symptoms of congestion such as shortness of breath or ankle swelling. Recent studies suggest that reducing the nerve activity to a kidney could reduce sodium retention and blood pressure. An improvement in the way the kidneys handle sodium may reduce disease progression and decrease symptoms for heart failure patients.

Study Overview

• Status: Terminated
• Conditions: Heart Failure
• Intervention / Treatment: Device: Symplicity Renal Denervation

Detailed Description

Over the past decades, clinical trials in HF have been unable to alter the natural history of cardio-renal compromise. Fluid retention accounts for the majority of admissions for acute decompensated heart failure, and salt and water removal using intravenous (IV) diuretics has been the mainstay of therapy applied to this population.1 Over 20% of hospitalized patients in the Acute Decompensated Heart Failure National Registry (ADHERE) had serum creatinine values greater than 2.0 mg/dL2 with the majority of congested patients presenting with significantly elevated systolic blood pressures rather than low-output states.1 Administration of IV loop diuretics further produces intravascular volume depletion and reduction in glomerular filtration rates3 as well as an increase in neurohormonal activation.4 This is true regardless of whether LVEF is impaired or preserved.5 However, despite relieving symptoms, acute drug administrations (such as adenosine receptor antagonists or natriuretic peptide analogues) for short durations have not changed the long-term cardio-renal outcomes in large clinical trials.

Recent recognition of different phenotypes of cardio-renal syndrome has provided better characterization of patient populations to evaluate specific treatment approaches or interventions.6 There is now greater appreciation that patients with congestive HF depend not only on an adequate glomerular function for renal glomerular filtration, but also on adequate tubular function for effective sodium handling that may or may not be dependent on glomerular filtration.7 Despite optimizing intracardiac filling pressures, many patients with August 28, 2013 Page 10 of 58 cardio-renal compromise remain symptomatic, complaining of breathlessness and fatigue often associated with concomitant increase in neurohormonal up-regulation (e.g. natriuretic peptides) and poor outcomes.8 Since the majority of patients present with hypertension, it points to the possibility that congestive HF is precipitated by heightened sympathetic drive.

Animal models have demonstrated that both blood pressure control and renal tubular function/glomerular filtration (as a function of renal blood flow) can be directly influenced by renal sympathetic nerve activity,9-12 which has evolved to provide cardiovascular support in the setting of hypovolemia or profound cardiovascular collapse. Specifically, HF animal models with denervated kidneys have demonstrated improvement in renal blood flow and natriuresis (with restoration of Na+-K+ ATPase at the loop of Henle, as well as epithelial sodium pumps at the distal tubules). However, our understanding of how persistently activated renal sympathetic outflow can lead to exaggerated neurohormonal up-regulation and chemoreceptor regulation in humans is still evolving. As heightened cardio-renal compromise leads to disease progression and congestive HF, it is conceivable that an approach to selectively modulate renal sympathetic outflow may improve cardio-renal compromise as well as the target mechanism leading to symptomatic improvement in at-risk patients.

By establishing the mechanistic role of renal sympathetic outflow in patients with impaired sodium handling as a contributor to congestion in HF, we may better understand why patients with HF develop symptoms, retain salt and water, and activate neurohormonal systems. This trial will be hypothesis generating and will serve to inform a larger clinical trial in patients with congestion related to HF.

The Data Safety and Monitoring Board (DSMB), an independent committee assigned by the sponsor to oversee the conduct and safety of this study, met on May 12, 2014 to review information that had become available from another study of the renal artery denervation procedure using the same investigational catheter as the PRESERVE study. Even though there were no concerns for the safety of subjects that had the renal artery denervation, the DSMB decided to stop the PRESERVE study.

Based upon agreement with the FDA, the protocol was amended to reduce subject participation from 52 weeks to 13 weeks and to only collect limited safety information.

• Study Type: Interventional
• Enrollment (Actual): 5
• Phase: Phase 2

Contacts and Locations

Study Locations

• United States
  • Georgia
    • Atlanta, Georgia, United States, 30322
      • Emory University
  • Massachusetts
    • Boston, Massachusetts, United States, 02114
      • Massachusetts General Hospital
    • Boston, Massachusetts, United States, 02130
      • Brigham and Women's Hospital
    • Boston, Massachusetts, United States, 02153
      • Tufts Medical Center
  • Minnesota
    • Rochester, Minnesota, United States, 55905
      • Mayo Clinic
  • Missouri
    • St. Louis, Missouri, United States, 63110
      • Washington University
  • North Carolina
    • Durham, North Carolina, United States, 27705
      • Duke University Medical Center
  • Ohio
    • Cleveland, Ohio, United States, 44195
      • Cleveland Clinic
    • Cleveland, Ohio, United States, 44115
      • Metro Health System
  • Pennsylvania
    • Philadelphia, Pennsylvania, United States, 19107
      • Thomas Jefferson University Hospital
    • Philadelphia, Pennsylvania, United States, 19104
      • University of Pennsylvania Health System
  • Vermont
    • Burlington, Vermont, United States, 05401
      • The University of Vermont - Fletcher Allen Health Care

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 21 years to 80 years (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Male or female, aged 21-80 years old.
• History of chronic HF (>6 months) with current NYHA II-III symptoms.
• Left Ventricular Ejection Fraction ≤40% on a clinically indicated echocardiogram obtained within 6 months prior to informed consent.
• Requires daily loop diuretic (≥40mg furosemide per day, or equivalent) to maintain euvolemia (absence of congestive signs including jugular venous distension with Jugular Venous Pressure > 7cm H20, ≥ moderate (2+) peripheral edema, S3).
• Optimized medical therapy for HF. Patients will be receiving guideline-recommended therapy (per the 2013 ACCF/AHA HF Guidelines) including angiotensin-converting enzyme (ACE) inhibitors and/or angiotensin receptor blocker, beta-blockers, and aldosterone antagonists without changes in heart failure medication regimen (including diuretics) for previous 14 days.
• Systolic blood pressure (BP) ≥110 mmHg at time of informed consent.
• Able to maintain stable medications for 52 weeks.
• Suitable renal artery anatomy for Renal Sympathetic Denervation (RSD) procedure. All of the following criteria must be met, based on the screening renal Doppler ultrasound:
• ≥ 20mm treatable length in each renal artery,
• Diameter in treatable segments must be ≥4mm,
• Lone main renal vessel feeding each kidney.

Exclusion Criteria:

• Unable to comply with protocol or procedures.
• Evidence of orthostatic hypotension or known dysautonomia. Orthostatic hypotension is defined by ≥1 of the following feature(s) within 2-5 minutes of quiet standing:
• ≥ 20 mmHg fall in systolic pressure
• ≥ 10 mmHg fall in diastolic pressure
• Symptoms of cerebral hypoperfusion (e.g. dizziness or lightheadedness, visual blurring or darkening of the visual fields, syncope).
• Evidence of or history of renal artery stenosis, nephrectomy, or renal transplant.
• Significant renal impairment as defined by estimated glomerular filtration rate (eGFR) < 45 ml/min/1.73m2 determined by Modification of Diet in Renal Disease (MDRD) equation.
• Significant proteinuria (>2g protein/daily protein excretion).
• Body mass index (BMI) >35 kg/m2.
• Acute coronary syndrome within last 4 weeks as defined by ECG changes and biomarkers of myocardial necrosis (e.g. troponin) in an appropriate clinical setting (chest discomfort or angina equivalent).
• Coronary revascularization procedures (percutaneous coronary intervention or cardiac artery bypass graft) and or valve surgery within 30 days of screening or expected procedures within the next 6 months.
• Cardiac resynchronization therapy, with or without implantable cardiac defibrillator within 90 days of screening or expected procedures within the next 6 months.
• Hypertrophic or restrictive cardiomyopathy, constrictive pericarditis, active myocarditis, active endocarditis, or complex congenital heart disease.
• Severe advanced HF, with ANY of the following features:
• Current or anticipated use of ventricular assist device within the next 6 months.
• Current or anticipated IV vasoactive drug therapy for HF management within the next 6 months.
• Listed cardiac transplant candidate, with transplantation likely within the next 6 months.
• Known allergic reactions to iodinated radiological contrast media or iodinated antiseptics.
• Greater than moderate mitral or aortic stenosis, and/or severe tricuspid regurgitation.
• Terminal illness (other than HF) with expected survival of less than 1 year.
• Female who is pregnant, nursing, or of childbearing potential not practicing effective birth control.
• Enrollment or planned enrollment in another clinical trial within the next 12 months.
• History of urinary outflow tract obstruction, bladder retention and/ or moderate to severe prostate hypertrophy.
• History of adrenal insufficiency
• History of untreated hypothyroidism
• Patients with non-cardiac dyspnea or fatigue due to frailty, motivational factors, pulmonary disease or orthopedic problems that precludes them from performing 6MWT (Six-Minute WalkTest).

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: None (Open Label)

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Other: Early Symplicity Renal Denervation; Subjects undergo Symplicity Renal Denervation within 2 weeks of baseline visit will follow usual care after week 13 visit	Device: Symplicity Renal Denervation; Renal denervation
Other: Late Symplicity Renal Denervation; Subjects following usual care until week 13 visit will then undergo Symplicity Renal Denervation within 2 weeks of Week 13 visit	Device: Symplicity Renal Denervation; Renal denervation

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Urine Sodium Excretion	Within-subject comparison of increase in urine sodium excretion following saline loading before RSD and 13 weeks following RSD.	13 Weeks following Renal Denervation

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Urine Volume	Urine volume following furosemide therapy after sodium loading.	13 Weeks following Renal Denervation
24-hour Urine Sodium Excretion	Difference in 24-hour urine sodium excretion, compared between pre-RSD and 13 weeks after RSD.	13 Weeks following Renal Denervation
Glomerular Filtration Rate	Estimated Glomerular Filtration Rate (GFR) by creatinine and cystatin C	13 Weeks following Renal Denervation
Serum Cystatin C	Study terminated early, endpoints not measured	13 Weeks following Renal Denervation
Blood Urea Nitrogen (BUN) Level	Study terminated early, endpoints not measured	13 Weeks following Renal Denervation
Creatinine Clearance From 24-hour Urine Creatinine	Study terminated early, endpoints not measured	13 Weeks following Renal Denervation
Urine Albumin	Urine albumin	13 Weeks following Renal Denervation
Renal Resistive Index	Intra-renal hemodynamics as measured by Renal Resistive Index (RRI) by renal Doppler ultrasonography Study terminated early, endpoints not measured	13 Weeks following Renal Denervation
Left Ventricular End Systolic Volume	Echo: Left ventricular end systolic volume Study terminated early, endpoints not measured	13 Weeks following Renal Denervation
Left Ventricular Ejection Fraction	Echo: Left Ventricular Ejection Fraction Study terminated early, endpoints not measured	13 Weeks following Renal Denervation
Global Longitudinal Strain	Echo: Global longitudinal strain Study terminated early, endpoints not measured	13 Weeks following Renal Denervation
LV End Systolic Dimension (LVESd)	Echo: LV end systolic dimension (LVESd)	13 Weeks following Renal Denervation
LV End Diastolic Dimension (LVEDd)	Echo: LV end diastolic dimension (LVEDd)	13 Weeks following Renal Denervation
Left Atrial Size	Echo: Left Atrial size	13 Weeks following Renal Denervation
Plasma N-terminal Pro-brain Natriuretic Peptide		13 Weeks following Renal Denervation
Resting Plasma Norepinephrine		13 Weeks following Renal Denervation
Resting Urine Norepinephrine		13 Weeks following Renal Denervation
Plasma Renin Activity		13 Weeks following Renal Denervation
Plasma Aldosterone		13 Weeks following Renal Denervation
6 Minute Walk Test		13 Weeks following Renal Denervation
Kansas City Cardiomyopathy Questionnaire Score		13 Weeks following Renal Denervation
Patient Global Assessment		13 Weeks following Renal Denervation
New York Heart Association (NYHA) Functional Classification		13 Weeks following Renal Denervation
Heart Rate Variability	Heart rate variability indices by Holter	13 Weeks following Renal Denervation
Tissue Doppler Indices	Echo: Tissue Doppler indices	13 Weeks following Renal Denervation
Left Ventricular End Diastolic Volume	Echo: Left Ventricular End Diastolic Volume	13 Weeks following Renal Denervation

Collaborators and Investigators

• Sponsor: Adrian Hernandez
• Collaborators: National Heart, Lung, and Blood Institute (NHLBI); Medtronic

Study record dates

Study Major Dates

• Study Start: December 1, 2013
• Primary Completion (Actual): December 1, 2014
• Study Completion (Actual): December 1, 2014

Study Registration Dates

• First Submitted: September 24, 2013
• First Submitted That Met QC Criteria: September 26, 2013
• First Posted (Estimate): October 1, 2013

Study Record Updates

• Last Update Posted (Estimate): February 2, 2016
• Last Update Submitted That Met QC Criteria: December 30, 2015
• Last Verified: December 1, 2015

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Heart Diseases; Cardiovascular Diseases; Heart Failure
• Other Study ID Numbers: Pro00047050; 5U10HL084904 (U.S. NIH Grant/Contract)