Actively Recruiting

Phase Not Applicable
Age: 18Years - 70Years
All Genders
NCT04391465

Assessment of the Relationship Between Cerebral Blood Flow and Heart Rate

Led by University of Calgary · Updated on 2026-05-07

20

Participants Needed

1

Research Sites

329 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The investigators will seek to determine the relationship between heart rate and middle cerebral artery (MCA) cerebral blood flow (CBF), as well as better understand the hemodynamic determinants of MCA CBF velocity. In order to manipulate heart rate, the investigators will recruit patients already scheduled for clinically indicated elective electrophysiological studies, where temporary pacing catheters placed in the right atrium can be used to artificially pace the heart at controlled rates. MCA CBF will be measured by transcranial Doppler ultrasound.

CONDITIONS

Official Title

Assessment of the Relationship Between Cerebral Blood Flow and Heart Rate

Who Can Participate

Age: 18Years - 70Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Male or female
  • Age 18-70 years, inclusive
  • Scheduled for clinically indicated elective electrophysiological studies where temporary pacing catheters are being placed in the right atrium
  • Left ventricular ejection fraction 6550%
  • Able and willing to provide informed consent
  • Able to travel to the Cardiac Electrophysiology Laboratory at the Foothills Medical Centre, Calgary, Alberta, Canada
Not Eligible

You will not qualify if you...

  • Unable or unwilling to provide informed consent
  • Other factors which in the investigator's opinion would prevent the participant from completing the protocol

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

Foothills Medical Center

Calgary, Alberta, Canada, T2N 4Z6

Actively Recruiting

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Research Team

S

Satish R Raj, MD MSCI

CONTACT

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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