Neurocognitive function G97.9 U51.02
Conditions
Interventions
Group 1: Group reversal NMB: MoCA, vital parameters, subjective condition evaluated by patient + observer, in each case pre-op and in the postoperative course 4 x up to 7 days post-op + follow-up.
Col
Sponsors
Universitätsklinikum Frankfurt Klinik für Anästhesiologie, Intensivmedizin und Schmerztherapie
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: ASA I-III, planned ITN, elective small to medium-sized surgery
Exclusion criteria
Exclusion criteria: Neurological disease with MoCA <26/30; polyneuropathy; chronic pain; use of retarded opioids; history of substance abuse; perioperative use of: clonidine, diphenhydramine, droperidol, ketamine, midazolam; perioperative transfusion; known pregnancy or lactation.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| neurocognitive assessment using the MoCA score (vs. 7.1-7.3 and 8.1-8.3) preOP, 0-15 min (Mini-MoCA), 3 times during the PACU stay, once before discharge, after 30 days | — |
Secondary
| Measure | Time frame |
|---|---|
| Subjective assessment of alertness, EEG change (alpha power), plasma level of fentanyl during the course, O2 saturation, | — |
Countries
Germany
Contacts
Public ContactSebastian Zinn
Universitätsklinikum Frankfurt Klinik für Anästhesiologie, Intensivmedizin und Schmerztherapie
Outcome results
None listed