ELR Monitoring Against Permanent Pacemaker in Atrial Fibrillation

NCT02506621 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2015-07-23

No results posted yet for this study

Summary

Randomised crossover study comparing the sensitivity and specificity of 5 External loop recorders in detecting pacemaker detected Atrial fibrillation burden.

Conditions

Interventions

DEVICE

R test

DEVICE

Nuubo

DEVICE

TECHNOMED pocket ECG

DEVICE

ZIO xt patch

DEVICE

MoMe

Sponsors & Collaborators

  • Eastbourne General Hospital

    lead OTHER

Principal Investigators

  • Neil Sulke, DM, FRCP · Eastbourne General Hospital

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-09-30
Primary Completion
2015-12-31
Completion
2016-01-31

More Related Trials

Entities

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 NCT02506621 on ClinicalTrials.gov