Processed EEG for Monitoring of Anesthetic Depth in Intracranial Tumor Surgery
Recruiting now · Not applicable
Conditions studied: Brain Tumor Adult, Processed EEG, Total Intravenous Anesthesia
In brief
An important feature of neurosurgical anesthesia is early postoperative recovery of consciousness with minimal residual sedation. This is a key factor to enable early neurological assessment and early discovery of postoperative complications. The goal of this single centre clinical trial is to compare propofol/remifentanil anesthesia delivered by manual total intravenous anesthesia (mTIVA) or target controlled infusion (TCI) for intracranial tumor resection via craniotomy. Anesthetic depth will be assessed by a simplified processed EEG (pEEG). The main question is time spent within recommended pEEG- levels from anesthesia induction until end of surgery. Secondary questions are: * mean pEEG-level, time from end of surgery to consiousness, * peroperative propofol/remifentanil consumption * postoperative degree of sleepiness * awareness assessment Participants are adults having have planned surgery for open resection of a brain tumor and will receive general anesthesia with propofol and remifentanil randomized to mTIVA or TCI. pEEG vill be blinded. * Participants will be asked to grade postoperative sleepiness using a specific scale * Follow up regarding awareness will be performed.
Key facts
- Study ID
- NCT06922500
- Run by
- Region Skane
- People needed
- 126
- Starts
- 2024-11-21
- Expected to finish
- 2027-07-01
- Last updated by the study team
- 2025-04-10
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Elective craniotomy for tumor resection
- Adult patient
- Consent to participation
You may not qualify if…
- Cognitive impact affecting infrmed consent
- brain tumor planned for biopsy without resection Tumor localisation not permitting placement of pEEG electrodes.
Where it is running
- Anesthesia and Intensive Care, Skane University Hospital — Lund, Sweden (enrolling)
Full record on ClinicalTrials.gov
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