VAgal Nerve Stimulation: safeGUARDing Heart Failure Patients

Last updated: March 12, 2018
Sponsor: LivaNova
Overall Status: Completed

Phase

2

Condition

Chest Pain

Heart Failure

Congestive Heart Failure

Treatment

N/A

Clinical Study ID

NCT02113033
NVNS01
  • Ages > 18
  • All Genders

Study Summary

The purpose of the VANGUARD study is to demonstrate the safety of Vagal Nerve Stimulation for the treatment of congestive heart failure with reduced ejection fraction, and to report secondary measures of efficacy.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. Left ventricular dysfunction of ischemic or idiopathic dilated cardiomyopathyetiology, characterized by LVEF < 40%

  2. Chronic heart failure with symptoms characterized by NYHA functional class II or IIIat the time of enrollment despite optimal drug regimen

  3. Optimal drug regimen as defined in the current European guidelines

  4. Sinus rhythm, with spontaneous heart rate ≥ 60bpm at the time of enrollment

  5. Signed and dated informed consent

Exclusion

Main Exclusion Criteria:

  • Patient implanted with or eligible to cardiac pacing as per current guideline

  • Risk for neck surgery in the electrode zone within a year after enrollment

  • Patient with right carotid artery stenosis

  • Symptomatic hypotension

  • History of peptic ulcer disease or upper gastrointestinal bleeding

  • Asthma, severe COPD, or severe restrictive lung disease

  • Advanced Diabetes Mellitus

  • Recent acute myocardial infarction, coronary artery surgery or revascularization (oralready planned)

  • Recent cerebro-vascular event

  • Significant valvulopathy

  • Advanced Renal failure

  • Previous heart transplant or current LVAD device therapy

  • Life expectancy < 1 year for non-cardiac cause

  • Patient included in another clinical study that could confound the results of thisstudy

  • Inability to understand the purpose of the study or to perform the procedures of thestudy

  • Unavailability for scheduled follow-up

  • Age of less than 18 years or under guardianship

  • Pregnancy

Study Design

Total Participants: 15
Study Start date:
October 07, 2014
Estimated Completion Date:
September 20, 2016

Connect with a study center

  • UCL St Luc

    Bruxelles, 1200
    Belgium

    Site Not Available

  • Hôpital Européen Georges Pompidou

    Paris, 75015
    France

    Site Not Available

  • CHRU Hôpital Pontchaillou

    Rennes, 35033
    France

    Site Not Available

  • CHU Rangueil

    Toulouse, 31059
    France

    Site Not Available

  • Rikshospitalet

    Oslo, 0027
    Norway

    Site Not Available

  • Dedinje Cardiovascular Institute

    Belgrade, 11040
    Serbia

    Site Not Available

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