Al Prediction of Sarcopenia Risk in Neurocritical ICU Patients

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-65
SponsorTrabzon Kanuni Education and Research Hospital

About this trial

This prospective observational study aims to evaluate sarcopenia in intensive care patients with intracranial pathologies using ultrasound and to compare the predictive performance of different artificial intelligence models. Rectus femoris muscle thickness will be measured by ultrasound on ICU admission (Day 0) and Day 7. Prealbumin levels will be assessed on Days 0, 3, and 7, and the modified Nutrition Risk in Critically Ill (mNUTRIC) score will be calculated on the first day of ICU admission. Clinical, laboratory, and ultrasonographic data will be integrated into different artificial intelligence models to predict sarcopenia status on Day 7. The study aims to determine the effectiveness of artificial intelligence in the early identification of sarcopenia and to support future clinical decision-making in intensive care practice.

Eligibility criteria

Qualifiers

Age between 18 and 65 years

Admission to the intensive care unit due to intracranial pathology (intracerebral hemorrhage, epidural hemorrhage, subdural hemorrhage, subarachnoid hemorrhage, intracranial tumors, or ischemic stroke)

Informed consent obtained from the patient or legally authorized representative

Disqualifiers

Age <18 years or >65 years

Failure to achieve nutritional targets according to ESPEN guidelines

Palliative care or home care patients

Morbid obesity (BMI ≥40 kg/m²)

Trial design

Treatments tested in this trial

  • Prospective Observational Assessment

Treatment groups

100 Participants
are divided into 1 treatment group