Status:
UNKNOWN
Efficacy of BIS Monitoring in Deep Hypnotic State
Lead Sponsor:
Indonesia University
Conditions:
Hypnotic; Withdrawal State With Delirium
Neurological Disorder
Eligibility:
All Genders
30-60 years
Phase:
NA
Brief Summary
Determining the efficacy of the BIS monitor in monitoring deep hypnotic states as well as intra- and post-operative outcomes in neurosurgery patients
Detailed Description
This study will be conducted with a two-group, double-blind, randomized clinical trial design in elective patients who will undergo neurosurgical procedures under general anesthesia. Patients schedule...
Eligibility Criteria
Inclusion
- Patients aged 30-60 years with an ASA tolerance of 1-2 who will undergo general anesthesia techniques
- Operation duration \> 3 hours
- The patient agrees to take part in the study.
Exclusion
- Continuous intraoperative use of ketamine, magnesium sulfate, dexmedetomidine, lidocaine agents
- Massive bleeding that causes hemodynamic disturbances
- Severe electrolyte disturbances
- Severe liver or kidney function disorders
- The patient was decided not to extubate in the operating room
Key Trial Info
Start Date :
December 15 2023
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
February 28 2024
Estimated Enrollment :
50 Patients enrolled
Trial Details
Trial ID
NCT06177847
Start Date
December 15 2023
End Date
February 28 2024
Last Update
December 20 2023
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