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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