OPS-2018 1-694 (Diagnostic laparoscopy (peritoneoscopy)) R11
Conditions
Interventions
Group 1: Control group:
General anesthesia including opioids as analgesic component
Group 2: Intervention group:
opioid-free anesthesia including adjuvants as analgesic component
Sponsors
Universitätsklinikum Münster, Klinik für Anästhesiologie, operative Intensivmedizin und Schmerztherapie
Eligibility
Sex/Gender
Female
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: -female sex -age >18years
Exclusion criteria
Exclusion criteria: -chronic pain -allergies or contradictions against the used anesthetic agents -pregnant or breastfeeding women
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| incidence of PONV up to 24h post-op | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. severity of PONV (simplified PONV impact scale, Myles et al (2012)) 2. postoperative opioid requirement 3. pain severity (NRS-Score) 4. postoperative recovery time 5. patient satisfaction 6. incidence of anesthesia awareness | — |
Countries
Germany
Contacts
Public ContactManuel Wenk
Universitätsklinikum Münster, Klinik für Anästhesiologie, operative Intensivmedizin und Schmerztherapie
Outcome results
None listed