Actively Recruiting
Assessing Systemic Circulation and LV Performance in Adults
Led by University of Calgary · Updated on 2026-05-05
100
Participants Needed
1
Research Sites
432 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Background There are significant limitations in the current approaches to assessing 2 important areas of cardiovascular physiology - the systemic circulation and left ventricular (LV) performance. The investigators' have repurposed the concepts of "systemic vascular conductance" to assess systemic circulation, and the "head capacity principle" to assess LV performance. The investigators' now seek to test these concepts in human adults, with heart failure and without heart failure, using non-invasive methods. Hypothesis There will be a depressed head-capacity curve and reduced power among patients with heart failure which will indicate compromised left ventricular pump function. Methods The research study will involve a single outpatient visit per subject. The study will take place with the subject supine on a bed/table. The subjects will be instrumented with EKG electrodes and finger blood pressure cuffs. The continuous finger BP device performs a waveform analysis in real-time to determine the non-invasive stroke volume, cardiac output, and blood pressure. The patient will be supine for at least 5 minutes to collect baseline data before being handed a dynamometer device. The subject will then be asked to squeeze the dynamometer with maximum force for a minimum of 2 minutes while only engaging their forearm and remaining relaxed in the rest of their body. The subject will then release the dynamometer and remain supine, in recovery, for a minimum of 5 minutes. Following the handgrip test, the instrumentation will be removed and the patient's participation in the study will be complete. The study duration should be about 20 min.
CONDITIONS
Official Title
Assessing Systemic Circulation and LV Performance in Adults
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or older
- Clinical heart failure (HFrEF or HFpEF) for heart failure patients
- No clinical heart failure for non-heart failure participants
You will not qualify if you...
- Unable or unwilling to provide informed consent
- Currently on intravenous inotrope or pressor medications to maintain cardiac function
AI-Screening
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Trial Site Locations
Total: 1 location
1
University of Calgary
Calgary, Alberta, Canada, T2N 4Z6
Actively Recruiting
Research Team
R
Rasha Hamzeh, RN
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
DIAGNOSTIC
Number of Arms
3
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