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Clinical Trials/NCT04005482
NCT04005482
Unknown
Not Applicable

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

Medical University of Vienna0 sites140 target enrollmentSeptember 20, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Atrial Fibrillation
Sponsor
Medical University of Vienna
Enrollment
140
Primary Endpoint
Mean and maximum blood pressure difference between before (baseline) and during/after medication.
Last Updated
6 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
September 20, 2019
End Date
July 20, 2021
Last Updated
6 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Hans Domanovits

Principal Investigator

Medical University of Vienna

Eligibility Criteria

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

Outcomes

Primary Outcomes

Mean and maximum blood pressure difference between before (baseline) and during/after medication.

Time Frame: 20th July 2019 to 20th July 2021

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