Atrial Fibrillation Prior and Post Elective Cardioversion
NCT ID: NCT05926401
Last Updated: 2023-11-30
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
150 participants
OBSERVATIONAL
2023-09-01
2025-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
OTHER
Study Groups
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Planned elective cardioversion for atrial fibrillation
ECG monitoring prior and after cardioversion
Continuous ECG monitoring at home 3-5 days prior to and 5-7 days after planned cardioversion
Interventions
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ECG monitoring prior and after cardioversion
Continuous ECG monitoring at home 3-5 days prior to and 5-7 days after planned cardioversion
Eligibility Criteria
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Inclusion Criteria
* Informed written consent for participation
Exclusion Criteria
* Pacemaker/CRT device
* No smart phone
18 Years
ALL
No
Sponsors
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Oslo University Hospital
OTHER
Sorlandet Hospital HF
OTHER_GOV
Responsible Party
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Principal Investigators
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Sigrun Halvorsen, PhD
Role: STUDY_CHAIR
Oslo university hospital /University of Oslo
Locations
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Sorlandet Hospital
Arendal, , Norway
Countries
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Central Contacts
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Facility Contacts
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Jarle Jortveit, PhD
Role: primary
Other Identifiers
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543834
Identifier Type: -
Identifier Source: org_study_id