💬In plain words
What the trial is, and whether it could suit you
This study aims to evaluate the effects of different postoperative analgesic approaches on postoperative delirium in elderly patients undergoing total knee arthroplasty.
Sign in to get the eligibility rules as simple questions to take to your doctor.
📋 Eligibility rules (as published)
Inclusion Criteria:
* Patients undergoing elective unilateral total knee arthroplasty under spinal anesthesia
* ASA physical status I-III
* Age ≥60 years
* Body mass index (BMI) between 18-30 kg/m²
* Preoperative fasting duration of approximately 8 hours
Exclusion Criteria:
* Refusal to participate in the study or inability to provide written informed consent
* American Society of Anesthesiologists (ASA) physical status IV or higher
* Obese patients (BMI \>30 kg/m²) or cachectic patients (BMI \<18 kg/m²)
* Patients requiring general anesthesia or in whom spinal anesthesia could not be achieved
* Contraindications to spinal anesthesia
* Emergency surgeries
* Psychiatric or neurological disorders causing cognitive dysfunction (e.g., epilepsy, schizophrenia, dementia, Alzheimer's disease)
* Use of psychotropic or opioid medications, or a history of alcohol abuse or withdrawal within the last 6 months
* Mini-Mental State Examination (MMSE) score ≤24
* Stage III-IV hepatic encephalopathy
* Severe impairments preventing cognitive assessment, such as blindness or severe hearing loss
* Patients meeting delirium criteria according to baseline 3D-CAM assessment or unable to complete the test
* History of cranio-cerebral surgery
* Acute myocardial infarction within the previous 12 months before surgery
* Requirement for postoperative intensive care unit admission
💊
What it tests
- adductor canal block and biFes block including bupivacain
- Periarticular infiltration
Ankara Bilkent City Hospital
Ankara, Turkey (Türkiye)
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.