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Fibrosis, Inflammation and Brain Health in Atrial Fibrillation. (NOR-FIB2)

University of Oslo (UIO) logo

University of Oslo (UIO)

Status

Completed

Conditions

Atrial Fibrillation
Stroke

Study type

Observational

Funder types

Other

Identifiers

NCT03816865
NOR-FIB2

Details and patient eligibility

About

Protocol synopsis Sponsor: Oslo University Hospital Title: Fibrosis, inflammation and cerebral infarction in patients with atrial fibrillation Study Design: The study is an observational prospective study of atrial fibrillation patients undergoing direct-current cardioversion.

Primary Objective: To assess the prevalence and causes of new silent cerebral ischemic lesions after programmed direct-current cardioversion using diffusion-weighted sequences in brain MRI (DWMRI).

Secondary Objectives:

To study the impact of inflammation measured by biomarkers and cardiac 18F-FDG-PET on the risk for new silent cerebral ischemic lesions after direct-current cardioversion for AF.

To assess the impact of fibrosis measured by biomarkers on the risk for new silent cerebral ischemic lesions after direct-current cardioversion for AF.

To assess cognitive and cerebral structural and metabolic changes after direct-current cardioversion for AF using cognitive assessments and cerebral and cardiac 18F-FDG-PET before and 12 months after treatment.

Number of Subjects: 50

Study Centers: Østfold Hospital Trust

Duration of Study Participation:

  • Enrollment: 18 months
  • Follow-up period: 12 months
  • Total Study Duration: 30 months

Primary Endpoints:

• Number of new small cerebral infarcts detected with DWMRI two weeks after direct current cardioversion.

Secondary Endpoints:

  • Rate of AF recurrence within 1 year after direct current cardioversion
  • Change in levels of inflammation biomarkersfrom baseline to 12 months follow-up
  • Change in levels of fibrosis biomarkers from baseline to 12 months follow-up
  • Cognitive function at 12 months follow-up
  • Changes in uptake pattern on cerebral 18F-FDG-PET from baseline to 12 months follow-up
  • Changes in uptake pattern on cardiac 18F-FDG-PET from baseline to 12 months follow-up
  • Brain volume at 12 months follow-up
  • White matter volume 12 months follow-up
  • Grey matter volume 12 months follow-up
  • Cortical volume 12 months follow-up
  • RSI-derived diffusion parameters 12 months follow-up: fast apparent diffusion coefficient, extracellular water fraction, fractional anisotropy; free water fraction; intracranial volume; NAWM: normal appearing white matter; neurite density; RSI: restriction spectrum imaging; sADC: slow apparent diffusion coefficient;restricted fractional anisotropy; white matter lesions.

Enrollment

46 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

  1. Known atrial fibrillation
  2. Age <80 years
  3. CHA2DS2-VASc ≤ 4
  4. Planned direct-current cardioversion

Exclusion criteria:

  1. CHA2DS2-VASc >4
  2. Life expectancy less than 1 year
  3. Patient otherwise not eligible for the study or adherent for follow-up (eg nonresident) or has concurrent disease affecting outcome (e.g. multiple sclerosis, cancer)

Trial contacts and locations

2

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Central trial contact

Anne Hege Aamodt, MD, PhD; Gudrun Høie, MD

Data sourced from clinicaltrials.gov

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