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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01823887
Other study ID # C-01
Secondary ID
Status Completed
Phase Phase 1/Phase 2
First received April 1, 2013
Last updated February 17, 2015
Start date July 2012
Est. completion date June 2014

Study information

Verified date February 2015
Source Cyberonics, Inc.
Contact n/a
Is FDA regulated No
Health authority India: Drugs Controller General of India
Study type Interventional

Clinical Trial Summary

The ANTHEM-HF Study is designed to demonstrate the safety and efficacy of vagus nerve stimulation (VNS) with the Cyberonics VNS Therapy System for the treatment of subjects with symptomatic heart failure.


Description:

Heart failure patients will be enrolled and randomized to cervical VNS implantation on either the left side or right side. After a 2-week post-implantation recovery period and a 10-week stimulation titration period, continuous periodic stimulation will be performed for 6 months, with data collection at 3 months and 6 months.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date June 2014
Est. primary completion date April 2014
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients with symptomatic heart failure, New York Heart Association (NYHA) class II/III with reduced EF and dilated hearts

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Device:
Vagus Nerve Stimulation (VNS)
Electrical Stimulation of the Vagus Nerve

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Cyberonics, Inc.

Country where clinical trial is conducted

India, 

References & Publications (2)

Dicarlo L, Libbus I, Amurthur B, Kenknight BH, Anand IS. Autonomic regulation therapy for the improvement of left ventricular function and heart failure symptoms: the ANTHEM-HF study. J Card Fail. 2013 Sep;19(9):655-60. doi: 10.1016/j.cardfail.2013.07.002. — View Citation

Premchand RK, Sharma K, Mittal S, Monteiro R, Dixit S, Libbus I, DiCarlo LA, Ardell JL, Rector TS, Amurthur B, KenKnight BH, Anand IS. Autonomic regulation therapy via left or right cervical vagus nerve stimulation in patients with chronic heart failure: — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Cardiac Function Left ventricular end-systolic volume (LVESV) and ejection fraction (EF) 6 months No
Primary Adverse Events Incidence of procedure and device-related complications 6 months Yes
Secondary Functional Status 6-minute walk test 6 months No
Secondary Quality of Life Minnesota Living with Heart Failure Questionnaire 6 months No
Secondary Functional Status New York Heart Association Class 6 months No
Secondary Autonomic Function Heart Rate Variability (HRV) 6 months No
Secondary Blood Biomarkers Blood Levels of Heart Failure Biomarkers 6 months No
Secondary Cardiac Function Left ventricular end-systolic diameter (LVESD) 6 months No
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