on-invasive model-based assessment of individual cardiovascular interactio

Completed

• Conditions: arteriosclerosis; high blood pressure; 10082206; 10003216

• Registration Number: NL-OMON35052
• Lead Sponsor: Medisch Universitair Ziekenhuis Maastricht

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 6 May 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 40

Inclusion Criteria

documented high blood pressure, age above 18

Exclusion Criteria

pregnancy, intended pregnancy, hypertensive urgency or emergency, cardiac arrhythmias, severe obesity precluding echo and tonometric assessment

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>1. Agreement between existing (clinically used) methods and newly developed<br /><br>methods for determining: arterial wall properties (distensibility as function<br /><br>of pressure) and left ventricular geometry (dilated or not, wall thickened or<br /><br>not).<br /><br><br /><br>2. Reproducibility of the new methods, which determines the ability to track<br /><br>changes in functional and structural aspects of cardiovascular interaction over<br /><br>time.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Possible contribution of the new methods to the clinical diagnosis and<br /><br>treatment of hypertensive patients. (By retrospective analysis by physician.)</p><br>