About this trial
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.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
elective vertebra surgery
aged 18-65
ASA score I-III
BMI <30 kg/m2
Disqualifiers
patient's refusal
BMI >30 kg/m2
serious liver or kidney disease
ASA 4 ve more
Trial population
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.
Trial design
Other
Prospective
Treatments tested in this trial
CHATGPT Group
Other interventionCHATGPT responses
GEMİNİ group
Other interventionGEMİNİ responses
COPİLOT group
Other interventionCOPİLOT responses
CLINICIAN group
Other interventionClinicians responses
Treatment groups
Trial outcomes
Primary outcomes
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.
Sponsors and contacts
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This trial is not recruiting at the moment. You can still explore other options: