Autonomic Neural Regulation Therapy to Enhance Myocardial Function in Heart Failure (ANTHEM-HF) Study (ANTHEM-HF)
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ClinicalTrials.gov Identifier: NCT01823887 |
Recruitment Status :
Completed
First Posted : April 4, 2013
Last Update Posted : February 19, 2015
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
Congestive Heart Failure | Device: Vagus Nerve Stimulation (VNS) | Phase 1 Phase 2 |
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 60 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | None (Open Label) |
Primary Purpose: | Treatment |
Official Title: | Autonomic Neural Regulation Therapy to Enhance Myocardial Function in Heart Failure (ANTHEM-HF) Study |
Study Start Date : | July 2012 |
Actual Primary Completion Date : | April 2014 |
Actual Study Completion Date : | June 2014 |

Arm | Intervention/treatment |
---|---|
Experimental: Left Sided Stimulation
Left cervical Vagus Nerve Stimulation (VNS)
|
Device: Vagus Nerve Stimulation (VNS)
Electrical Stimulation of the Vagus Nerve |
Experimental: Right Sided Stimulation
Right Cervical Vagus Nerve Stimulation (VNS)
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Device: Vagus Nerve Stimulation (VNS)
Electrical Stimulation of the Vagus Nerve |
- Cardiac Function [ Time Frame: 6 months ]Left ventricular end-systolic volume (LVESV) and ejection fraction (EF)
- Adverse Events [ Time Frame: 6 months ]Incidence of procedure and device-related complications
- Functional Status [ Time Frame: 6 months ]6-minute walk test
- Quality of Life [ Time Frame: 6 months ]Minnesota Living with Heart Failure Questionnaire
- Functional Status [ Time Frame: 6 months ]New York Heart Association Class
- Autonomic Function [ Time Frame: 6 months ]Heart Rate Variability (HRV)
- Blood Biomarkers [ Time Frame: 6 months ]Blood Levels of Heart Failure Biomarkers
- Cardiac Function [ Time Frame: 6 months ]Left ventricular end-systolic diameter (LVESD)

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Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Patients with symptomatic heart failure, New York Heart Association (NYHA) class II/III with reduced EF and dilated hearts

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01823887
India | |
Chennai, India |
Study Director: | Imad Libbus, PhD | Cyberonics, Inc. |
Other Publications:
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: | Cyberonics, Inc. |
ClinicalTrials.gov Identifier: | NCT01823887 |
Other Study ID Numbers: |
C-01 |
First Posted: | April 4, 2013 Key Record Dates |
Last Update Posted: | February 19, 2015 |
Last Verified: | February 2015 |
Heart Failure Vagus Nerve VNS |
Heart Failure Heart Diseases Cardiovascular Diseases |