Actively Recruiting
Assessment of Stroke Volume and Cardiac Output in Response to Varying Heart Rates and Body Position - a Pacemaker Based Study
Led by University of Calgary · Updated on 2026-05-05
25
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are studying how different heart rates affect stroke volume and cardiac output in patients with vasovagal syncope who have permanent pacemakers. This study aims to clarify how increasing heart rate impacts the heart's ability to fill with blood and pump effectively, both when lying down and when upright. The investigation addresses a gap in understanding the relationship between heart rate and cardiac function in this group. The study involves pacing the heart at various rates ranging from 50 to 130 beats per minute while monitoring stroke volume and cardiac output using non-invasive methods. After completing pacing runs while lying down, participants rest for 10 minutes before being tilted upright at an angle greater than 70 degrees for about 10 minutes, followed by additional pacing sessions. Blood pressure is measured and the equipment calibrated between pacing runs. Participants will undergo assessments that include continuous monitoring of stroke volume and cardiac output during different pacing rates and positions. The primary outcome is the change in cardiac output during atrial pacing at different rates while lying down. Secondary outcomes include changes in cardiac output and stroke volume during various pacing modes and body positions. The entire study procedure occurs within one day, and safety is ensured by using non-invasive techniques and secure positioning during upright testing.
CONDITIONS
Brief Title
Assessment of Stroke Volume and Cardiac Output in Response to Varying Heart Rates
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18-70 years (inclusive)
- Implanted permanent pacemaker or implanted defibrillator capable of atrial and ventricular pacing
- Left ventricular ejection fraction greater than 50%
You will not qualify if you...
- Unable or unwilling to provide informed consent
- Clinical need for a cardiac resynchronization device
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 1 day
Participants undergo pacing at multiple heart rates while lying down and then upright to assess stroke volume and cardiac output responses. The procedure includes calibration of a finger blood pressure cuff and a tilt test to simulate standing.
1 day of continuous assessment with paced heart rate adjustments and positioning
Trial Site Locations
Total: 1 location
1
University of Calgary
Calgary, Alberta, Canada, T2N 4Z6
Actively Recruiting
Research Team
S
Satish R Raj, MD MSCI
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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