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Bispectral Index, Suppression Rate and Emergence Agitation in Spine Surgeries

NCT06334939 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 94

Last updated 2024-10-24

No results posted yet for this study

Summary

Emergence agitation; generally refers to a situation that may occur after a surgical intervention or anesthesia. This situation describes the irritability and agitation of the patient during the recovery process and the period of recovery from anesthesia. Recovery agitation may occur when the patient begins to recover and is usually a short-term condition. It resolves spontaneously. However, in some cases, this agitation may be more pronounced and disturbing. This may affect the patient\'s condition and relaxation. Rapid recovery from anesthesia in the clinic is also a risk factor for agitation.

When the literature is examined, there are not enough studies on Bis suppression ratio and its relationship with recovery agitation is not yet known enough. For this purpose, our study aimed to question this relationship.

Conditions

  • Emergence Agitation
  • Anesthesia Recovery
  • Bispectral Index Monitor

Interventions

DEVICE

Bispectral Index Monitoring

Study patients will undergo perioperative bispectral index and BIS suppression ratio (SR) monitoring under anesthesia. The lowest BIS and BIS SR values and the values taken at 10-minute intervals will be recorded throughout the case. The Richmond agitation scale will be calculated in the recovery room after anesthesia.

Sponsors & Collaborators

  • Ahmet Yuksek

    lead OTHER_GOV

Principal Investigators

  • Ahmet YUKSEK, MD · Kocaeli City Hospital

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-01-01
Primary Completion
2024-08-01
Completion
2024-08-30

Countries

  • Turkey (Türkiye)

Study Locations

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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 NCT06334939 on ClinicalTrials.gov