Stopped: Too long recruitment period due to small number of patients
This study will examine the effect of intraoperative sedation with midazolam, propofol and dexemdetomidine on the occurrence of postoperative cognitive impairment in patients undergoing surgical treatment of pertrochanteric fracture of the femur.
Age range
65 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Occurrence of postoperative cognitive dysfunction (POCD) measured by MMSE
Timeframe: 5 days
Occurrence of postoperative cognitive dysfunction (POCD) measured by DSST
Timeframe: 5 days
Postoperative inflammation measured by serum CRP levels
Timeframe: 5 days
Postoperative inflammation measured by white blood cells count
Timeframe: 5 days
Postoperative inflammation measured by serum IL-6 levels
Timeframe: 5 days
Postoperative inflammation measured by serum cholinesterase activity
Timeframe: 5 days
Postoperative inflammation measured by serum PCT levels
Timeframe: 5 days