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Health Consequences of the Burden of Atrial Fibrillation (SwissAF-BURDEN)

University Hospital Basel logo

University Hospital Basel

Status

Completed

Conditions

Atrial Fibrillation
Burden

Study type

Observational

Funder types

Other

Identifiers

NCT05389228
Swiss-AF-BURDEN

Details and patient eligibility

About

The Swiss-AF-BURDEN study will be embedded in the follow-up visits of the Swiss-AF cohort study. The research question of the current atrial fibrillation burden will be answered by using 7-day Holter-ECG recordings and continuous implanted loop recorder recording, whereas cardiac MRI examination will give results about cardiac dimensions and function. The 7-day Holter ECG will be repeated after one year. The cMRI will be performed separately or directly after the brain MRI to minimize the additional burden for the patients. Only a subsample of 100 patients will additionally receive ILR for 2 years.

Enrollment

325 patients

Sex

All

Ages

45+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Swiss-AF study patient
  • Paroxysmal or persistent AF

Exclusion criteria

  • Permanent AF
  • Swiss-AF patients not willing or able to undergo 7-day Holter monitoring
  • Specifically for cMRI: Pregnant women or women of child-bearing age without a prior negative pregnancy test

Trial contacts and locations

1

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Central trial contact

Michael Kuehne, MD Prof, exec MBA; Rebecca Paladini, PhD

Data sourced from clinicaltrials.gov

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