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Clinical Trials/DRKS00006219
DRKS00006219CompletedNot Applicable

Extension of the EUROBservational Research Programme Atrial Fibrillation General Registry (EORP AFIB registry) for Germany - AFNET-EORP registry Atrial Fibrillation Germany

Die Register-Studie wird durchgeführt vom: Kompetenznetz Vorhofflimmern AFNET e.V.0 sites3,528 target enrollmentStarted: July 23, 2014Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
3,528

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Observational

Eligibility Criteria

Ages
18 Years to one (—)
Sex
All

Inclusion Criteria

  • Patients will be officially enrolled in the study only if ECG diagnosis of AF has been made.
  • - The qualifying episode of AF should have occurred within one year before the date of baseline.
  • - AF is the primary or secondary diagnosis, i.e. the current admission / visit may be due to other reasons.
  • - Patients need not be in AF at the time of enrolment.
  • - Signed Patient Inform Consent
  • - Age <= 18 years

Exclusion Criteria

  • Patients who are currently or are planned to be taking part in a cardiac clinical trial.
  • Please note that patients can participate concomitantly in other registries.

Investigators

Sponsor
Die Register-Studie wird durchgeführt vom: Kompetenznetz Vorhofflimmern AFNET e.V.

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