Actively Recruiting

Phase Not Applicable
Age: 18Years - 70Years
All Genders
ID03446326

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

Age: 18Years - 70Years
All Genders

Eligibility Criteria

Eligible

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%
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

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

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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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