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Clinical Trials in Canada / NCT03446326
Recruiting Not applicable

Assessment of Stroke Volume and Cardiac Output in Response to Varying Heart Rates

NCT03446326 · tracked via the Priya Life Science Canada tracker
Phase
Not applicable
Started
2018-01-01
Last updated
2026-05-05

Condition(s) studied

Vasovagal Syncope

Investigational drug(s) / intervention(s)

Pacing

Pacing: Assess the non-invasively determined stroke volume and cardiac output response at different paced heart rates in patients with a cardiac pacemaker or implanted defibrillator with preserved ejection fractions (LVEF≥50%)

Study summary

The investigators will seek to determine the effects of different heart rates on both stroke volume and cardiac output using non-invasive hemodynamic assessments. In order to safely manipulate the HR, the investigators will study patients with permanent pacemakers in whom heart rate manipulation can be done in a safe and non-invasive manner.

Eligibility

Sex
ALL
Min age
18 Years
Max age
70 Years
Healthy volunteers
No
Inclusion Criteria: * Age 18-70 years (inclusive) * Implanted permanent pacemaker or implanted defibrillator capable of atrial and ventricular pacing * LV ejection fraction \>50% Exclusion Criteria: * Unable or unwilling to provide informed consent * Clinical need for a cardiac resynchronization device

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
University of Calgary Calgary Alberta Recruiting

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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 NCT03446326 on ClinicalTrials.gov ↗ ← All trials in Canada