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
100 participants
OBSERVATIONAL
2021-09-25
2027-12-20
Brief Summary
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Detailed Description
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At inclusion patients undergo an in-depth interview regarding comorbidities, medication, previous treatments related to the AF diagnosis. In addition, baseline data for weight and height are collected.
In connection to inclusion the patients are asked leave venous bloodwork (Na, K, Creatinine, plasma Glucose and NTproB-Type Natriuretic Peptide). An echocardiographic exam is performed according to a prespecified protocol with special emphasis on the left atrial function and anatomy. This is followed by a continuous ECG recording for 14 days using BioTel ePatch. The ECG patch is later returned to a core facility by mail.
The patients´ are followed for five years and are asked to leave bloodwork and perform a 14-day ECG recording yearly. After these exams, a follow up phone call is placed to the patient aimed at documenting clinical progress related to symptoms, treatment and interventions. After 5 years follow up patients undergo a follow up echocardiographic exam in addition to yearly bloodwork and ECG recording. The patients´ clinical symptoms are treated at the clinician´s discretion according to current guidelines.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Diagnosis of atrial fibrillation within one year of inclusion
Exclusion Criteria
* Acute stressor for atrial fibrillation such as: acute ischemic heart disease or infection
18 Years
50 Years
ALL
No
Sponsors
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Boehringer Ingelheim
INDUSTRY
Karolinska Institutet
OTHER
Responsible Party
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Piotr Sobocinski Doliwa
Principal Investigator
Principal Investigators
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Piotr Sobocinski Doliwa, MD, PhD
Role: STUDY_CHAIR
Karolinska Institutet Danderyds University Hospital
Locations
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Danderyd Hospital
Stockholm, , Sweden
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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2021-00992
Identifier Type: -
Identifier Source: org_study_id
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