Surrogates for blood pressure tracking in critical care setting
Recruiting
- Conditions
- cardiovascular diseases
- Registration Number
- NL-OMON19922
- Lead Sponsor
- Philips Electronics Nederland B.V.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 40
Inclusion Criteria
•Patients admitted to the ICU with arterial line as standard of care
•Patients who undergo surgery (OR) with an arterial line as standard of care
•Age >18
•Patients who give their consent for the investigation
Exclusion Criteria
•Neuro-trauma
•Obesity (BMI>40)
•Pregnancy
•Delirium (diagnosed by hospital)
•Significant language barrier that prevents the patient from understanding the Informed Consent
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Investigation if surrogate parameters such as Pulse Arrival Time (PAT) can be used to track blood pressure changes.
- Secondary Outcome Measures
Name Time Method p to beat-to-beat tracking of blood pressure using initiated blood pressure surrogates in critical care patients in OR and ICU versus invasive blood pressure measurements.