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Autonomic Regulation Therapy in Heart Failure With Preserved Ejection Fraction

Not Applicable
Completed
Conditions
Congestive Heart Failure
Interventions
Device: Vagus Nerve Stimulation (VNS)
Registration Number
NCT03163030
Lead Sponsor
Cyberonics, Inc.
Brief Summary

The ANTHEM-HFpEF 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 with preserved and mid-range ejection fraction.

Detailed Description

Heart failure patients will be enrolled and implanted with a cervical VNS system on the right side. After a 2-week post-implantation recovery period and a 10-week stimulation titration period, continuous periodic stimulation will be performed for 12 months, with data collection at 3, 6, 9, and 12 months.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
52
Inclusion Criteria

Patients with symptomatic heart failure, New York Heart Association (NYHA) class II/III with preserved and mid-range EF (≥40%).

Exclusion Criteria

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
TherapyVagus Nerve Stimulation (VNS)Right Cervical Vagus Nerve Stimulation (VNS)
Primary Outcome Measures
NameTimeMethod
Adverse Events12 months

Incidence of procedure and device-related complications

Secondary Outcome Measures
NameTimeMethod
Cardiac Size (LAVI)12 months

Left atrial volume index

Quality of Life Score12 months

Minnesota Living with Heart Failure Questionnaire score

Cardiac Function (E/E')12 months

Ratio of mitral velocity to early diastolic velocity of the mitral annulus

Cardiac Size (LV mass index)12 months

Left ventricular mass index

Blood Biomarkers12 months

Blood Levels of Heart Failure Biomarkers (NT-proBNP, creatinine, C-reactive protein)

Functional Status (NYHA Class)12 months

New York Heart Association classification

Autonomic Function (HRV)12 months

Heart rate variability

Functional Status (6MWD)12 months

6-minute walk distance

Trial Locations

Locations (1)

Krishna Institute of Medical Science

🇮🇳

Secunderabad, India

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