Validation of a Propofol Detector (EDMON) for Anesthesia during a Single Lung Ventilation (SLV) Surgery
- Conditions
- Patients undergoing lung surgery with single-lung ventilation
- Registration Number
- DRKS00014788
- Lead Sponsor
- Center of Breath Research Klinik für Anästhesiologie, Intensivmedizin und Schmerztherapie Universitätsklinikum des Saarlandes
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 30
Written consent of the patient; Patients undergoing elective surgery for general anesthesia who require single-lung ventilation for surgical reasons; an arterial cannula is required for the procedure and / or postoperative care; Age = 18 years; ASA I-III; No significant hepatic, nephrological, neurological and cardiac pre-existing conditions; BMI <35; No participation in another study (up to 30 days before enrollment in the study); In women of childbearing potential: negative pregnancy test, or surgical sterilization or contraceptive use during the examination or min. 2 years after postmenopause
Contraindications or known intolerance to any of the medicines or procedures used; Pre-existing conditions or patient circumstances that make it impossible or meaningless to examine the patient (for example, dementia, psychiatric disorders, lack of understanding of speech or ability to speak); Patients with significant cardiac pre-existing conditions; Body Mass Index > 35; ASA status> III; drug abuse; Positive HIV or hepatitis test; Pregnancy; Rejection by the patient
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Determination of propofol concentration in the exhaled air during one-lung ventilation (ELV) compared to two-lung ventilation
- Secondary Outcome Measures
Name Time Method Comparison of propofol concentration in exhaled air during one-lung ventilation (ELV) versus blood plasma concentration.