Postoperative Delirium and Analgesia in Elderly Patients
- NCT ID
- NCT07849517
- Registry status
- Not yet recruiting
- Study type
- Interventional
- Phase
- Not applicable
- Sponsor
- Ankara City Hospital Bilkent
- Conditions
- Postoperative Delirium, Postoperative Pain, Acute
Overview
ClinicalTrials.gov lists this study as Not yet recruiting.
Official title: Effects of Different Analgesic Approaches on Postoperative Delirium in Elderly Patients Undergoing Total Knee Arthroplasty
Enrollment: 300 participants (Estimated).
What is being studied
- Drug: adductor canal block and biFes block including bupivacain
- Drug: Periarticular infiltration
Who may be eligible
- Ages
- 60 Years to no maximum
- Sex
- All
- Healthy volunteers accepted
- Yes
ClinicalTrials.gov lists the following eligibility criteria.
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
Study locations
No study locations are listed in the registry data.
Study details
- Start date
- October 1, 2026
- Primary completion date
- May 25, 2027
- Completion date
- June 15, 2027
- First posted
- September 30, 2026
Source and update information
- Source
- ClinicalTrials.gov
- NCT ID
- NCT07849517
- Registry last updated
- September 30, 2026
- QualifiedStudies registry data refreshed
- October 5, 2026
- QualifiedStudies record fetched
- October 5, 2026
View NCT07849517 on ClinicalTrials.gov
Trial information can change. Confirm current study details with the study team or the registry.
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