Long-term Pacemaker Arrhythmia Analysis

February 10, 2015 updated by: Neil Sulke, Eastbourne General Hospital

East Sussex Long-term Pacemaker Arrhythmia Analysis

Investigators seek to observe the long term patterns of arrhythmias detected by permanent pacemakers.

Study Overview

Status

Completed

Conditions

Study Type

Observational

Enrollment (Actual)

2551

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • E Sussex
      • Eastbourne, E Sussex, United Kingdom, BN21 2UD
        • Eastbourne General Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Those with permanent pacemakers

Description

Inclusion Criteria:

  • Pre-existing dual chamber permanent pacemaker

Exclusion Criteria:

  • Nil

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Permanent pacemaker
Pre-existing permanent pacemakers

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Atrial fibrillation burden
Time Frame: 28 days to 1 year
Proportion of monitored time in atrial fibrillation
28 days to 1 year

Secondary Outcome Measures

Outcome Measure
Time Frame
Atrial fibrillation episode frequency
Time Frame: 28 days to 1 year
28 days to 1 year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

June 1, 2014

Primary Completion (Actual)

February 1, 2015

Study Completion (Actual)

February 1, 2015

Study Registration Dates

First Submitted

December 11, 2013

First Submitted That Met QC Criteria

December 16, 2013

First Posted (Estimate)

December 20, 2013

Study Record Updates

Last Update Posted (Estimate)

February 12, 2015

Last Update Submitted That Met QC Criteria

February 10, 2015

Last Verified

February 1, 2015

More Information

Terms related to this study

Other Study ID Numbers

  • ESHT Pacemaker analysis

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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