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BLITZ Atrial Fibrillation

BLITZ Atrial Fibrillation

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03653598
Acronym
BLITZ-AF
Enrollment
4125
Registered
2018-08-31
Start date
2016-02-01
Completion date
2017-12-31
Last updated
2023-09-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Atrial Fibrillation

Keywords

Atrial Fibrillation

Brief summary

Management strategies for AF have made many advances over the last decade but there is still a great heterogeneity in the management of AF and it remains unclear how often clinicians adhere to current guidelines. A survey of an updated AF management would enable a timely assessment of implementation of current International guidelines, allow monitoring of early management of AF when a patients is admitted in a Emergency Room (ER) and Cardiology Unit.

Detailed description

Multicentre, observational study. 200 Italian Hospitals fully representing the Italian cardiology reality in terms of geographical distribution and level of hospital technology. Data collection in ER: Data on AF and Atrial Flutter episodes in ER will be collected retrospectively by checking the records of ER without collection of any data that can allow to identify the patients. These data will be collected under the responsibility of the Cardiology Departments consecutively for 4 weeks. Data collected in Cardiology: these data will be collected under the responsibility of the Cardiology Departments for 12 weeks consecutively.

Interventions

OTHERAtrial Fibrillation

Data collection on Atrial Fibrillation

Sponsors

Heart Care Foundation
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* All patients with AF, admitted to cardiology wards for an urgent or planned hospitalization. * All patients admitted in a Day Hospital regimen for treatment of AF The diagnosis of AF must be confirmed by ECG. * Signed Patient Inform Consent.

Exclusion criteria

* The qualifying episode of AF was not documented with an ECG. * Age \<18 years. * Patients with AF as a complication of an acute coronary syndrome (within 1 week from symptoms onset). * Patients with AF associated with cardiothoracic surgery (within 1 week from surgery). * Concomitant participation in other studies that can modify the diagnostic and/or therapeutic treatments. * Patients already enrolled in BLITZ-AF

Design outcomes

Primary

MeasureTime frameDescription
Rate or rhythm control strategyBaselane study completion - average 1 weekPercentage of patients in rate or thythm control therapy
Number of admissions of patients with AFEnrollemntNumber of admissions to the ER and cardiology wards of patients with AF
Antithrombotic strategiesBaselane study completion - average 1 weekRate of use of oral antithrombotic strategies

Secondary

MeasureTime frameDescription
Admission to the ER for atrial flutterEnrollmentNumber of admission to the ER for atrial flutter
Patients regularly followed up by the cardiology centers12 monthsRate of patients regularly followed up by the cardiology centers
Adherence to the 1A recommendations of current guidelines12 monthsRate of adherence to the 1A recommendations of current guidelines

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026