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NCT04809701

Non-vascular ICD Electrode Configuration Feasibility Study

Evaluation of Different Defibrillation Electrode Configurations for Development of a Non-vascular ICD
Abbott Medical Devices·ClinicalTrials.gov·procedureEnrolling by invitation
View on ClinicalTrials.gov →
Study focus
Disease/Condition
Ventricular Arrythmia
Drug/Device/Intervention
Temporary implantation of defibrillation coils and pulse generator
Study type
Interventional
Intervention type
procedure
Sponsor & location
Primary sponsor
Abbott Medical Devices
Location
Concepción,Prague,Asunción, Chile,Czech,Paraguay
Timeline & enrollment
Phase
N/A
Start date
Mar 22, 2021
End date
Aug 31, 2022
Enrollment
30 participants
Primary outcome

The rate of successful defibrillation of induced VA using each of the two NV-ICD electrode configurations

Summary

This study is designed to evaluate the energy requirements of two different Nonvascular ICD
 (NV-ICD) electrode configurations for achieving successful defibrillation of ventricular
 arrhythmias.

ICD-10 classifications
Ventricular tachycardiaLeft ventricular failureVentricular septal defectCardiomyopathy, unspecifiedCardiac arrhythmia, unspecified
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT04809701
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT04809701 through Pure Global AI's free database. This phase not specified trial is sponsored by Abbott Medical Devices and is currently Enrolling by invitation. The study focuses on Ventricular Arrythmia. Target enrollment is 30 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.