Investigation of the Hemodynamic Cardiac Profiler in assessing cardiac indices and clinical performance during exercise and cardiac stress
Recruiting
- Conditions
- stable ischemic heart disease
- Registration Number
- NL-OMON23429
- Lead Sponsor
- Hemologic B.V.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
Healthy volunteers aged 18 and older (phase 1,2) and stable ischemic heart disease patients and cardiac rehabilitation completed (phase 3)
Exclusion Criteria
symptomatic heart failure, inability or any contraindication to perform physical exercise, unstable ischemic heart disease, planned coronary revascularization, any significant valve pathology (grade >2), history of any open heart surgery, any chest malformation, any metal implants in the thoracic area
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method two way random intraclass correlation coefficient and the associated 95% CI of the four measurements of change in stroke volume slope using the HCP during CPX in healthy volunteers and in patients.
- Secondary Outcome Measures
Name Time Method