Trial of Autonomic neuroModulation for trEatment of Chronic Heart Failure

NCT ID: NCT01820130

Last Updated: 2019-02-04

Basic Information

• Recruitment Status: WITHDRAWN
• Clinical Phase: NA
• Study Classification: INTERVENTIONAL
• Study Start Date: 2013-03-31
• Study Completion Date: 2016-09-30

Brief Summary

The purpose of this clinical investigation is to evaluate the safety and efficacy of Spinal Cord Stimulation (SCS) in advanced heart failure (HF) patients with Implantable Cardioverter Defibrillator (ICD) but not indicated for Cardiac Resynchronization Therapy (CRT).

Conditions

Heart Failure

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Spinal Cord Stimulation system therapy

St Jude Medical EON mini rechargeable system

Group Type: EXPERIMENTAL

St Jude Medical EON mini rechargeable system

Intervention Type: DEVICE

implantation of Eon Mini Neurostimulation System (IPG Model 3788)

Interventions

St Jude Medical EON mini rechargeable system

implantation of Eon Mini Neurostimulation System (IPG Model 3788)

Intervention Type: DEVICE

Other Intervention Names

Eon Mini Neurostimulation System (IPG Model 3788)

Eligibility Criteria

Inclusion Criteria

• Patients has a Left Ventricular Ejection Fraction (LVEF) less than or equal to 35%
• Patient is in New York Heart Association (NYHA) Class III
• Patient has a QRS duration <120 ms (non-paced QRS, at the time of device Implant or protocol inclusion)
• Patient has had an ICD implanted for >90 days
• Patient is receiving stable and optimal medical therapy for HF (>90 days) as describe by "European Society of Cardiology 2012 recommendation for diagnosis and treatment of acute and chronic Heart Failure", except in case of contraindication or allergy
• Patient is able to provide written Informed Consent prior to any investigational related procedure

Exclusion Criteria

• Patient currently has an implanted spinal cord stimulator or previously had an implanted spinal cord stimulator which is now explanted or has had previous spinal surgery that would interfere with implant of percutaneous SCS leads in the upper thoracic region
• Patient has polyneuropathy
• Patient requires short-wave diathermy, microwave diathermy or therapeutic ultrasound diathermy
• Patient is in NYHA class IV
• Patient has received a tissue / organ transplant or is expected to have a tissue / organ transplant within the next 180 days
• Patient has a cardiac resynchronization therapy (CRT) device, or LV Assist device or is expected to receive CRT, or left ventricular assist device (LVAD) within the next 180 days
• Patient has critical valvular heart disease that requires valve repair or replacement
• Patient has had a myocardial infarction (MI) or cardiac revascularization procedure (percutaneous coronary intervention or coronary artery bypass graft) within 90 days of enrollment
• Patient is on IV inotropic therapy
• Patient has active myocarditis or early postpartum cardiomyopathy
• Patient has taken any of the following drugs within 30 days of enrollment: systemic corticosteroids, cytostatic and immunosuppressive drug therapy (cyclophosphamide, methotrexate, cyclosporine, azathioprine, etc.), DNA depleting or cytotoxic drugs
• Patient is pregnant, or of childbearing potential and is not using adequate contraceptive methods, or nursing
• Patient with a bleeding tendency (INR >1.2 and platelet count <100 x109 per liter)
• Patient has a local infection at the ICD implant location or systemic infection
• Patient has renal insufficiency (creatinine >3.0 mg/dl)
• Patient with risk of allergy to SCS device component materials
• Patient having one of the following condition must be considered as non relevant for SCS implantation:

1. / Patient with active stent

2. / Patient having bare metal stent for less than 6 months

3. / Patient presented with an acute coronary syndrome within the last 6 months

4. / Patient with stent on the common

5. / Patient with a history of stent thrombosis

6. / Coronary Patient receiving double antiplatelet medication

• Patient is participating in another clinical study with an active treatment arm
• Patient is less than 18 years old
• Patient's life's expectancy is less than 1 year as assessed by investigators

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Abbott Medical Devices

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Pierre Bordachar, MD

Role: PRINCIPAL_INVESTIGATOR

University Hospital, Bordeaux

Locations

CHU

Pessac, , France

Countries

France

Other Identifiers

CR-12-047-FR-SC

Identifier Type: -

Identifier Source: org_study_id