postoperative pain
Conditions
Interventions
Group 1: The SPI or NOL value is recorded at the end of the surgery. The correlation of the NOL/SPI value with the occurance of postsurgical pain is then analyzed.
Sponsors
Universitätsklinikum Schleswig-Holstein
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients with elective planned surgery in balanced general anesthesia (intubation anesthesia or laryngeal mask) using sevoflurane and sufentanil or in total intravenous anesthesia (TIVA) using propofol and sufentanil.
Exclusion criteria
Exclusion criteria: - Age under 18 years - Postoperative monitoring in the intensive care unit - atrial fibrillation - AV block> 1 degree - pacemaker - severe peripheral neuropathy - pregnancy - lack of consent - legal support
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint of this study is the prediction of pain levels and opioid demand in the recovery room based on the measurement results of the NOL monitor intraoperative. | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Correlates the NOL with the SPI at the end of the surgery (wound closure) 2. Correlates the NOL at the end of the surgery (wound closure) with hemodynamic parameters such as heart rate and blood pressure. 3. Are there age-specific differences when estimating the postoperative pain level using the NOL / SPI. 4. Are there gender differences when estimating postoperative pain levels using the NOL / SPI. 5. Are there differences between the assessment of postoperative pain using NOL / SPI under balanced anesthesia (sevoflurane + opioid) and totally intravenous anesthesia (propofol + opioid) | — |
Countries
Germany
Contacts
Public ContactLars Hummitzsch
Klinik für Anästhesiologie und operative Intensivmedizin, Universtitätsklinikum Schleswig Holstein, Campus Kiel
Outcome results
None listed