Bispectral Index in Patients Undergoing Vertebral Surgery Using Artificial Intelligence Programs: A Methodological Study
BIS
INTERPRETATION AND EVULATION OF THE PROXIMITY TO CLINICAL EXPERIENCE OF BISPECTRAL INDEX (BIS) IN PATIENTS UNDERGOİNG VERTEBRAL SURGERY USING ARTIFICIAL INTELLIGENCE PROGRAMS: A METHODOLOGICAL STUDY
1 other identifier
observational
63
1 country
1
Brief Summary
This study aims to interpret the Bispectral Index (BIS) monitoring method, which we routinely use for monitoring in scoliosis surgery, with artificial intelligence (AI) tools and to determine the accuracy and reliability of AI tools in clinical practice by comparing this interpretation with the interpretations of two clinicians experienced in BIS.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Jun 2026
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
June 9, 2026
CompletedStudy Start
First participant enrolled
June 10, 2026
CompletedFirst Posted
Study publicly available on registry
June 16, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 10, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 10, 2026
June 24, 2026
June 1, 2026
3 months
June 9, 2026
June 22, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Clinical Experience
The proximity of AI programs to the clinical experience. The study will examine the percentage of times AI programs' interpretations and intervention recommendations regarding information processing stimulus (ISIS) are identical to those of two clinical practitioners.
12 hours
Study Arms (4)
CHATGPT Group
GEMİNİ Group
COPİLOT Group
CLINICIAN Group
Interventions
Eligibility Criteria
Patients aged 18-65 years with ASA scores I-III and BMI \<30 kg/m2 who are scheduled for elective vertebra surgery will be included.
You may qualify if:
- elective vertebra surgery
- aged 18-65
- ASA score I-III
- BMI \<30 kg/m2
You may not qualify if:
- patient's refusal
- BMI \>30 kg/m2
- serious liver or kidney disease
- ASA 4 ve more
- anatomical abnormality at probe site
- history of mental or neurological disease,
- history of previous intracranial aneurysm or intracranial tumor surgery
- history of moderate or severe pulmonary disease,
- emergency surgery
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Health Sciences, Antalya Training and Research Hospital
Antalya, Muratpaşa, Turkey (Türkiye)
Study Officials
- PRINCIPAL INVESTIGATOR
Tayfun Sugur
University of Health Sciences, Antalya Training and Research Hospital
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
June 9, 2026
First Posted
June 16, 2026
Study Start
June 10, 2026
Primary Completion (Estimated)
September 10, 2026
Study Completion (Estimated)
December 10, 2026
Last Updated
June 24, 2026
Record last verified: 2026-06
Data Sharing
- IPD Sharing
- Will not share