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ICD Shock Detection by a Wearable

NCT04565652 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2021-03-23

No results posted yet for this study

Summary

Trial to assess the ability of a wearable to detect defibrillation from an implantable ICD

Conditions

  • Cardiac Arrest
  • Heart Arrest
  • Cardiopulmonary Arrest

Interventions

DEVICE

Device Wearers

The intervention arm will wear the LOIS ICD Smartband during routine ICD defibrillation following elective ICD implant.

Sponsors & Collaborators

  • Lois Medical LTD

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-03-03
Primary Completion
2021-11-30
Completion
2021-12-31

Countries

  • United Kingdom

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 NCT04565652 on ClinicalTrials.gov