A non-invasive Cardiac Output measurement as a replacement of the test bolus technique during CT
Completed
- Conditions
- Alle patienten die komen voor CT abdomen.n.v.t.
- Registration Number
- NL-OMON37655
- Lead Sponsor
- Jeroen Bosch Ziekenhuis
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 50
Inclusion Criteria
Referred for CTA of the abdominal aorta according to clinical indications
Mentally competent
Signed informed consent
* 18 years
Kidney function * 60 GFR
Exclusion Criteria
< 18 years
Mentally incompetent
Kidney function < 60 GFR
Allergy contrast medium
Known arrhythmias or other heart disorders
Pregnancy or lactation
16,9 * BMI * 30,1
Study & Design
- Study Type
- Observational invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>- The cardiac output, measured by the Nexfin Monitor.<br /><br>- The time delay, starting when the contrast medium is injected until the time<br /><br>that de necessary amount of Hounsfield Units is reached.</p><br>
- Secondary Outcome Measures
Name Time Method <p>- The correlation coefficient between the cardiac output and the delay time.</p><br>