Pregabalin Versus Dexmedetomidine for Delirium Prevention After Cardiac Surgery
Pregabalin, Dexmedetomidine, Delirium
About this trial
This is an interventional prevention trial for Pregabalin
Eligibility Criteria
Inclusion Criteria: ≥ 65 years of age both genders American Society of Anesthesiologists (ASA) physical status classification II or III scheduled for cardiac surgery. Exclusion Criteria: Patients who had history of psychiatric diseases; inability to communicate; previous history of POD; preoperative sick sinus syndrome. Allergy/sensitivity to pregabalin or dexmedetomidine. Severe bradycardia (heart rate <50 beat per minute). Second-degree or above atrioventricular block without pacemaker. Severe hepatic or renal insufficiency. Previous cardiac or thoracic surgery. Known diagnosis of depression or other major psychiatric diseases. Cognitive impairment or inability to cooperate with the study. Renal insufficiency, and history of substance abuse.
Sites / Locations
- Tanta UniversityRecruiting
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
pregabalin group
dexmedetomidine group
patients will receive pregabalin capsules (75 mg) will be given 2 h prior to induction of anesthesia and every 12 h for 24h postoperatively by nasogastric tube or orally. Patients will receive IV saline as placebo with the same rate of dexmedetomidine.
patients in the dexmedetomidine group will receive after induction of GA a bolus dose of 0.4 μg/kg dexmedetomidine (over a period of 10 to 20 min) followed by an infusion of 0.2 to 0.7 μg/kg/h. Patients will receive placebo 2 h prior to induction of anesthesia and every 12 h for 24h postoperatively by nasogastric tube or orally. If patients are hemodynamically unstable, the bolus dose will be omitted. The infusion of dexmedetomidine will be continued for a maximum period of 24 h. Dexmedetomidine infusion will be not discontinued before extubation.