R52.9
Conditions
Interventions
Group 1: We are going to collect data from patients undergoing general anesthesia during surgical intervention using EEG during and 30-90 days after the procedure.
Sponsors
Arbeitsgruppe Humane Schmerzmodelle, Fraunhofer IME - Institutsteil TMP
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: healthy subjects that are scheduled for a standardized surgical procedure without any expected complications, no persistent chronical pain, no administration of opioids for the past 5 days prior to the procedure
Exclusion criteria
Exclusion criteria: Allergy/intolerance to planned medication (anesthetics and analgesics), known polyneuropathy (e.g. diabetic, vascular, neurodegenerative), peripheral sensibility disorder, psychiatric disorder with an influence on pain sensation (e.g. severe depression, generalized anxiety disorder, self mutilation), ongoing administration or therapy with nonsteroidal antiinflammatory drugs in the past 5 days, drug abuse (alcohol, marihuana, cocaine, heroine etc.), sensible subjects (e.g. prisoners, minors, severely disabled people, homeless people), pregnancy and nursing period
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Characterization of EEG patterns that result from painful sensation in subjects | — |
Countries
Germany
Contacts
Public ContactMalte Anders
Arbeitsgruppe Humane Schmerzmodelle, Fraunhofer IME - Institutsteil TMP
Outcome results
None listed