Advanced non-invasive monitoring for individual and patient-adapted anesthesia management
Phase 2
- Conditions
- Malignant neoplasm of prostateMalignant neoplasm of liver and intrahepatic bile ductsMalignant neoplasm of oesophagusOther peripheral vascular diseasesC25I74Malignant neoplasm of kidney, except renal pelvisArterial embolism and thrombosisC26C22
- Registration Number
- DRKS00033353
- Lead Sponsor
- Klinik für Anästhesiologie, operative Intensiv- und Schmerzmedizin Universitätsmedizin Mannheim
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 530
Inclusion Criteria
• ASA class I-IV
• Patients from the aforementioned specific areas
• Signed consent form for participation in the stud
Exclusion Criteria
• Emergency procedures
• Mental impairment that prevents the patient from understanding the nature, extent, and significance of the research project
• Muscular dystrophies, myasthenias
• Cardiac arrhythmia
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Total opioid amount (intraoperative + in the recovery room + during hospitalization) in milligrams, morphine equivalent and<br>Postoperative pain control assessed using the Numerical Rating Scale (NRS) and QUIPS questionnaire.
- Secondary Outcome Measures
Name Time Method • Postoperative delirium monitoring / Qualitative awareness assessed using SBI (Sedation-Behavioral-Inventory).<br>• Time to extubation<br>• Postoperative duration of hospital stay<br>• Time in an Intensive Care Unit / Intermediate Care Unit (IMC)<br>• Noradrenaline requirement in milligrams<br>• Total intravenous infusion volume in milliliters<br>• Crystalloids in milliliters<br>• Colloids in milliliters<br>• Transfusions (PRBC, FFP, Platelets) in milliliters<br>• Total blood loss in milliliters