Actively Recruiting

Phase Not Applicable
Age: 40Years +
All Genders
Healthy Volunteers
NCT07343895

Population-based Atrial Fibrillation Screening in Individuals With NT-proBNP Above Median in the Tromsø Study

Led by University Hospital of North Norway · Updated on 2026-01-15

4000

Participants Needed

2

Research Sites

487 weeks

Total Duration

On this page

Sponsors

U

University Hospital of North Norway

Lead Sponsor

U

UiT The Arctic University of Norway

Collaborating Sponsor

AI-Summary

What this Trial Is About

The aim is to investigate whether screening with long-term ECG monitoring in individuals with elevated NT-proBNP leads to a lower incidence of ischeamic stroke and death from vascular causes. The project is a sub-study within the 8th wave of the population based Tromsø Study. Information on previous diseases, medication use, and risk factors is collected through questionnaires, blood samples, and measurements of height, weight, blood pressure, and ECG. A total of 4,000 individuals with NT-proBNP levels above the median, without previously known atrial fibrillation (AF) or ongoing anticoagulation therapy, will be randomized to either long-term heart rhythm monitoring (7 days) or a control group without long-term ECG monitoring (2,000 in each group). Individuals with AF in the intervention group will be offered anticoagulation therapy in accordance with current guidelines. The intervention group and the control group will be compared with regards to incident stroke and death within a 6-year follow-up period. Information on endpoints and anticoagulation use will be obtained through linkage to national registries.

CONDITIONS

Official Title

Population-based Atrial Fibrillation Screening in Individuals With NT-proBNP Above Median in the Tromsø Study

Who Can Participate

Age: 40Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 40 years or older
  • NT-proBNP above the median level
  • Informed consent for participation
Not Eligible

You will not qualify if you...

  • History of atrial fibrillation (self-reported)
  • Current use of anticoagulation therapy
  • Presence of pacemaker or cardiac resynchronization therapy (CRT) device
  • No available smartphone

AI-Screening

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Trial Site Locations

Total: 2 locations

1

Uit The Arctic University of Norway

Tromsø, Norway, 1902

Actively Recruiting

2

University Hospital of North Norway Health Trust

Tromsø, Norway

Actively Recruiting

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Research Team

A

Agnethe Eltoft, MD, PhD

CONTACT

E

Emelia Gjesvik

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SCREENING

Number of Arms

2

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