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NCT05926401 Clinical Trial

Atrial Fibrillation Prior and Post Elective Cardioversion

Atrial Fibrillation Clinical Trial

Official title:
Atrial Fibrillation Prior and Post Elective Cardioversion

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT05926401
Other study ID # 543834
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date September 1, 2023
Est. completion date December 31, 2025

Study information
Verified date November 2023
Source Sorlandet Hospital HF
Contact Jarle Jortveit, PhD
Phone +4799450714
Email jarle.jortveit@sshf.no
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Cardioversion from atrial fibrillation (AF) to sinus rhythm (SR) is performed primarily to improve patient symptoms. However, due to the intermittent nature of AF, patients may have converted to SR prior to elective cardioversion and the recurrence rate of AF after cardioversion can be high. The aims of this study are to assess the rate of spontaneously conversion to SR in patients with AF scheduled for elective cardioversion, as well as the rate of early recurrence of AF after elective cardioversion.

Recruitment information / eligibility
Status Recruiting
Enrollment 150
Est. completion date December 31, 2025
Est. primary completion date June 30, 2024
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Planned elective cardioversion of AF - Informed written consent for participation Exclusion Criteria: - Lack of ability to cooperate - Pacemaker/CRT device - No smart phone

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• ECG monitoring prior and after cardioversion
Continuous ECG monitoring at home 3-5 days prior to and 5-7 days after planned cardioversion

Locations
Country Name City State
Norway Sorlandet Hospital Arendal

Sponsors (2)
Lead Sponsor Collaborator
Sorlandet Hospital HF Oslo University Hospital

Country where clinical trial is conducted

Norway, 

Outcome
Type Measure Description Time frame Safety issue
Primary The rate of spontaneously conversion to SR in patients with AF scheduled for elective cardioversion 10 days pre/post cardioversion
Primary The rate of early recurrence (<5 days) of AF after elective cardioversion up to 5 days pre/post cardioversion
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