DRKS00023188CompletedNot Applicable
Continuous and non-invasive determination of blood pressure: a triple comparison in clinical practice
Klinik und Poliklinik für Anästhesiologie, Zentrum für Anästhesiologie und Intensivmedizin, Universitätsklinikum Hamburg-Eppendorf0 sites60 target enrollmentStarted: October 2, 2020Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Enrollment
- 60
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Observational
Eligibility Criteria
- Ages
- 18 Years to one (—)
- Sex
- All
Inclusion Criteria
- •Patients scheduled for elective surgery who require invasive BP monitoring with an intra-arterial catheter placed in the A. radialis for clinical indications unrelated to the study
- •Adult patients (patients aged = 18 years)
Exclusion Criteria
- •Patients with pronounced edema in the hands
- •Patients with vascular implants at the sites of non-invasive BP measurement (fingers and upper arms, respectively)
- •Patients with pronounced disturbance of peripheral blood circulation (peripheral artery disease of Fontaine state II and above, Raynaud syndrome, a-v-shunt etc.)
- •Patients with tonic seizures and/or excessive movements
- •Patients with history of arrhythmias
- •Patients with arteriosclerosis
- •Patients with atrial fibrillation
- •Patients with valvular disease of grade 2 or above
- •Patients with cardiac assist devices
- •Patients who, in addition to invasive BP monitoring, require NIBP measurements unrelated to the investigational devices
- •Patients who obtain vasoactive medications on the same arm as used for upper-arm NIBP measurements from the NiCCI System
- •Patients with a large lateral difference in BP (> 15 mmHg for systolic BP and/or >10 mmHg for diastolic BP) or with same arm measurement differences > 10mmHg in systolic or diastolic BP during assessment of lateral differences
- •Capillary refill-time > 2 seconds
Investigators
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