Ireland
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Recruiting Observational

Left-atrial Fibrosis in Persistent Atrial Fibrillation and Its Comorbidities

NCT07857044 · tracked via the Priya Life Science Germany tracker
Sponsor
Christina Berr. MD
Phase
Observational
Started
2023-03-31
Last updated
2026-10-05

Condition(s) studied

Atrial FibrillationSleep ApneaPrimary Aldosteronism

Investigational drug(s) / intervention(s)

Screening on comorbidites

Screening on comorbidites: Patients with persistent atrial fibrillation that undergo ablation are screened for comorbidities

Study summary

Pulmonary vein isolation is an established intervention for atrial fibrillation. Patients with a paroxysmal atrial fibrillation have no or only few comorbidities and a good prognosis in respect to their atrial fibrillation. In contrast, patients with persistent atrial fibrillation often suffer from relevant comorbidities and recurrence of atrial fibrillation is common. Left-atrial fibrosis and its electrophysiological consequences are involved in the recurrence rate, but pathophysiological mechanisms are yet to be better characterized. The study investigates relevant comorbidities to elucidated their effect on atrial fibrosis and recurrence rates of atrial fibrillation. Furthermore, the investigators evaluate the prevalence of these comorbidities.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * persistent atrial fibrillation, eligible for ablation * BMI 19-40 Exclusion Criteria: * valvular atrial fibrillation * formerly ablation * medication interfereing with measurements of atrial fibrosis * known or treated comorbidities (OSAS, PA)

Primary outcome measure(s)

  • quantification of area of left-atrial fibrosis in the heart — baseline
    During ablation elecrical maping of the left-atrium is done and percentage of left-atrial fibrosis (electrical tissue abnormalities) will be assessed
  • Rate of recurrence of atrial fibrillation (yes/no) in the study group — 1 year after procedure (ablation)
    measure the recurrence of AF in follow-up with holter-ekgs

Trial sites (1)

FacilityCityRegionStatus
University hospital Augsburg Augsburg Bavaria Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07857044 on ClinicalTrials.gov ↗ ← All trials in Germany