Efficacy of BIS Monitoring in Deep Hypnotic State

Launched by INDONESIA UNIVERSITY · Dec 10, 2023

Keywords

ClinConnect Summary

This clinical trial is looking at a device called the BIS monitor, which helps doctors track how deeply a patient is under anesthesia during surgery. The goal is to see if using this monitor can improve the care of patients undergoing neurosurgery, particularly in terms of their recovery and any confusion or delirium they might experience afterward.

To participate in the study, patients need to be between 30 and 60 years old and fit a specific health status. They should be having surgery that lasts longer than three hours under general anesthesia. However, certain patients are not eligible, such as those who are receiving specific medications or have serious health issues affecting their blood pressure, electrolytes, liver, or kidneys. If someone joins the study, they can expect close monitoring during their surgery and will contribute to important research that could help improve outcomes for future patients. The trial is not yet recruiting participants, but it aims to gather valuable information about the effects of anesthesia on recovery after surgery.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • 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 Criteria:
• • 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