Anesthesia for carpal tunnel syndrome G56.0
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Be included in the study 160 male and female patients who are undergoing elective outpatient surgery of the upper extremity. In each case, 40 patients will be enrolled, who receive anesthesia as general anesthesia, an axillary brachial plexus block, an IV regional anesthesia or infiltration anesthesia
Exclusion criteria
Exclusion criteria: No suitability for anesthesia
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| - Process time: Implementing anesthesia to release anesthesia, cut / weld time, OP end up recording the recovery room - Effectiveness of anesthesia Sensory / motor testing of the surgical area, measurement of sympathetic blockade on the basis of skin resistance - Measurement of sympathetic activity (electrical sympatho graphy) intraoperatively by the change in skin resistance - Questionnaire Postoperatively (after surgical day / 2 days) Satisfaction school grade, preoperative pain (scale Nummeric rating scale 1-10), intraoperatively, postoperatively, 1day, 2day, regimen analgesics, adjunctive Postoperative nausea and vomiting, pain puncture site | — |
Secondary
| Measure | Time frame |
|---|---|
| Perioperative complications - anesthetic protocol Hemodynamic stability - anesthesia protocol | — |
Countries
Germany
Contacts
Universitätsmedizin Göttingen Zentrum Anästhesiologie, Rettungs- und Intensivmedizin