Phase
Condition
Vascular Diseases
Dizzy/fainting Spells
Circulation Disorders
Treatment
Continuous finger-cuff arterial pressure monitoring
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
We will include three types of patients:
Patients scheduled for ambulatory (outpatient) elective non-cardiac surgery expected to last ≥30 minutes
Low-risk patients (ASA I+II) having inpatient elective non-cardiac surgery expected to last ≥60 minutes
Moderate-risk patients (ASA III) having inpatient elective non-cardiac surgery expected to last ≥60 minutes
We will only include patients who are 18 years or older; who will have general anesthesia; and in whom intermittent arterial pressure monitoring with upper-arm cuff oscillometry is planned.
Patients that meet one or more of the following exclusion criteria cannot participate in the trial:
Emergency surgery
Patients on renal replacement therapy
Contraindications for finger-cuff monitoring (e.g., Raynaud disease)
Study Design
Study Description
Connect with a study center
University Medical Center Hamburg-Eppendorf
Hamburg,
GermanyActive - Recruiting
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