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NCT02016950 Clinical Trial

Long-term Pacemaker Arrhythmia Analysis

Atrial Fibrillation Clinical Trial

Official title:
East Sussex Long-term Pacemaker Arrhythmia Analysis

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02016950
Other study ID # ESHT Pacemaker analysis
Secondary ID
Status Completed
Phase N/A
First received December 11, 2013
Last updated February 10, 2015
Start date June 2014
Est. completion date February 2015

Study information
Verified date February 2015
Source Eastbourne General Hospital
Contact n/a
Is FDA regulated No
Health authority United Kingdom: National Health Service
Study type Observational

Clinical Trial Summary

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

Recruitment information / eligibility
Status Completed
Enrollment 2551
Est. completion date February 2015
Est. primary completion date February 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Pre-existing dual chamber permanent pacemaker

Exclusion Criteria:

Study Design

Observational Model: Cohort, Time Perspective: Retrospective

Related Conditions & MeSH terms

Locations
Country Name City State
United Kingdom Eastbourne General Hospital Eastbourne E Sussex

Sponsors (1)
Lead Sponsor Collaborator
Eastbourne General Hospital

Country where clinical trial is conducted

United Kingdom, 

Outcome
Type Measure Description Time frame Safety issue
Primary Atrial fibrillation burden Proportion of monitored time in atrial fibrillation 28 days to 1 year No
Secondary Atrial fibrillation episode frequency 28 days to 1 year No
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