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Bispectral Index and Surgical Field

Laparoscopy Clinical Trial

Official title:
Does Bispectral Index Improve Surgical Conditions During Fast Track Gynecological Benign Laparoscopies

Clinical Trial Summary

This study investigates whether BIS monitor assisted anesthesia improves surgical space conditions during gynecological benign laparoscopic procedures. Half of participants will receive BIS monitor assisted anesthesia, while the other half will receive anesthesia without BIS monitor.

Clinical Trial Description

General Anesthesia includes hypnosis/unconsciousness, amnesia, analgesia, muscle relaxation and autonomic and sensory blockade of responses to noxious stimulation. Depth of anesthesia in standard practice is controlled by monitoring equipment such as blood pressure (BP), heart rate (HR), train of four ratio (TOF) and by clinical signs such as profuse sweating, tearing, cough and movements. BIS can be used as additional tool to monitor and manage anesthesia. BIS is an empirically derived scale for measuring brain electrical activity. It computes an index between 0 and 100, whereas 0 corresponds to "no detectable brain electrical activity" (flatline EEG) and 100 to awake state. A patient is considered to be appropriately anesthetized when the BIS' value is between 40 and 60. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03911544
Study type Interventional
Source Aalborg University Hospital
Contact
Status Completed
Phase N/A
Start date April 1, 2019
Completion date March 11, 2021
View Details
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