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Blood Pressure During Rate Control in Patients With Tachycardic Atrial Fibrillation at the Emergency Department

Blood Pressure During Rate Control in Patients With Tachycardic Atrial Fibrillation at the Emergency Department

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04005482
Acronym
BPIRCTPTAF
Enrollment
140
Registered
2019-07-02
Start date
2019-09-20
Completion date
2021-07-20
Last updated
2019-09-17

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

Conditions

Atrial Fibrillation

Brief summary

The aim of this study is to analyse blood pressure during rate control therapy in patients with tachycardic atrial fibrillation in a real-world emergency cohort.

Detailed description

Atrial fibrillation (AF) is the primary clinical problem in 3.3% to 10.0 % emergency department (ED) admissions. Rate control is an integral part of the management of symptomatic tachycardic AF patients. According to the recent guidelines beta-blockers, digoxin, the calcium channel blockers diltiazem and verapamil, amiodarone or combination therapy should be considered for rate control. Haemodynamic side-effects in particular hypotension may occur. Heart rate and blood pressure behavior in an ED population during rate control therapy in patients with tachycardic atrial fibrillation will be analysed.

Interventions

Rate control according to the Atrial fibrillation - ESC Guidelines 2016

Sponsors

Medical University of Vienna
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 120 Years
Healthy volunteers
No

Inclusion criteria

* Age \> 18 years * Atrial fibrillation or atrial flutter and heart rate ≥ 110 bpm * Indication for rate control * Informed consent

Exclusion criteria

• Inclusion criteria not met

Design outcomes

Primary

MeasureTime frame
Mean and maximum blood pressure difference between before (baseline) and during/after medication.20th July 2019 to 20th July 2021

Contacts

Primary ContactJan Niederdöckl, Dr.med.univ
jan.niederdoeckl@meduniwien.ac.at0043 40400 19640
Backup ContactFilippo Cacioppo
filippo.cacioppo@meduniwien.ac.at0043 40400 19640

Outcome results

None listed

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