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Cardiac Output Autonomic Stimulation Therapy for Acute Heart Failure (COAST-AHF)

NCT03169803 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2018-08-23

No results posted yet for this study

Summary

A feasibility study to investigate the safety and performance of the NeuroTronik Cardiac Autonomic Nerve Stimulation (CANS) Therapy System

Conditions

  • Heart Failure Acute

Interventions

DEVICE

NeuroTronik CANS Therapy™ System

The NeuroTronik CANS Therapy™ System is a percutaneous, catheter-based, bedside electrical stimulation system. The System consists of the single-use, disposable NeuroCatheter™ and NeuroCatheter™ Placement Kit, along with the reusable, bedside NeuroModulator™ Development System, and the NeuroTronik CANS Therapy™ Cable.

Sponsors & Collaborators

  • NeuroTronik Inc.

    lead INDUSTRY

Principal Investigators

  • Temístocles Díaz, MD · Hospital Punta Pacífica, Panama City, Panama

Study Design

Allocation
NA
Purpose
DEVICE_FEASIBILITY
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-05-19
Primary Completion
2019-05-19
Completion
2019-06-19

Countries

  • Panama

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03169803 on ClinicalTrials.gov