MedTrace Logo

Efficacy of BIS Monitoring in Deep Hypnotic State

NCT06177847 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2023-12-20

No results posted yet for this study

Summary

Determining the efficacy of the BIS monitor in monitoring deep hypnotic states as well as intra- and post-operative outcomes in neurosurgery patients

Conditions

  • Hypnotic; Withdrawal State With Delirium
  • Neurological Disorder
  • Postoperative Delirium
  • Postoperative Confusion
  • Anesthesia
  • Anesthesia Emergence Delirium
  • Gas; Inhalation

Interventions

DEVICE

BIS

In the group with BIS where the anesthesia protocol is opened, namely the use of anesthetic gas, the anesthetic drug will be adjusted to the BIS value range of 40-60 or BIS-guided

Sponsors & Collaborators

  • Indonesia University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
30 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-12-15
Primary Completion
2024-01-30
Completion
2024-02-28

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06177847 on ClinicalTrials.gov