Phase
Condition
Mental Disability
Dementia
Memory Loss
Treatment
No Pericapsular nerve group block
Pericapsular nerve group block
Clinical Study ID
Ages > 65 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Patients who will undergo surgery with spinal anesthesia due to total hipreplacement
ASA (American Society of Anesthesiologists) I-II-III patients
Patients aged 65 and over
Patients with a preoperative fasting period of approximately 8 hours
Exclusion
Exclusion Criteria:
Refusal to participate in the study
ASA (American Society of Anesthesiologists) score of 4 and above
Body mass index >40 kg/m²)
Failure of spinal block
Patients who underwent surgery with general anesthesia
Patients who received preoperative and intraoperative sedation
Patients who will undergo revision surgery
Patients with a history of drug use
Patients with psychiatric disorders or those taking antipsychotic medications (depression, bipolar disorder, schizophrenia, etc.)
Patients with central nervous system disease (Alzheimer's disease, Parkinson'sdisease, multiple sclerosis, etc.)
Patients who do not accept spinal anesthesia and/or pericapsular nerve group (PENG)block
Patients with a preoperative Mini Mental Test (MMT) score below 25
Patients with contraindications for regional anesthesia techniques
Patients who developed perioperative delirium
Patients with visual or hearing impairment
Patients who require blood or blood product transfusion during surgery
Patients who cannot cooperate in the postoperative period
Study Design
Study Description
Connect with a study center
Ankara Bilkent City Hospital
Çankaya, Ankara 06530
TurkeySite Not Available

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