Ketofol for Preventing Postoperative Delirium in Elderly Patients
Delirium on Emergence
About this trial
This is an interventional prevention trial for Delirium on Emergence focused on measuring ketofol, dexmedetomidine, post operative delirium, elderly patients
Eligibility Criteria
Inclusion Criteria:
- Patient acceptance.
- Age ≥ 60 years old.
- American society of anesthesia (ASA) (II-III).
- Gender: males &females
- BMI < 35kg/m2.
- able to communicate verbally.
- Scheduled for exploration surgery for intestinal obstruction under general anesthesia of at least 60 min duration
Exclusion Criteria:
- Patient refusal.
- Patients with delirium prior to surgery.
- Patients with drug misuse history or taking anti-psychotic drugs.
- Previous hospitalization within 3 months.
- Legal blindness, severe deafness.
- History of Acute cerebrovascular conditions; stroke or transient ischemic attack.
- Patients who could not be prepared with proper fluid resuscitation, electrolyte and acid-base correction prior to surgery.
- Patients who could be discharged from the intensive care unit (ICU) within two days.
- Patients with a known history of allergy to study drugs
Sites / Locations
- Faculty of medicine, zagazig university
Arms of the Study
Arm 1
Arm 2
Arm 3
Placebo Comparator
Active Comparator
Active Comparator
Control group
ketofol group
dexmedetomidine group
21 ml of normal saline 0.9% will be I.V continuously infused fifteen minutes after induction of anesthesia up to two hours postoperatively.
21 ml of a mixture of (ketamine and propofol) will be I.V continuously infused fifteen minutes after induction of anesthesia up to two hours postoperatively
21 ml of a mixture of (dexmedetomidine diluted with normal saline 0.9%) will be I.V continuously infused fifteen minutes after induction of anesthesia up to two hours postoperatively