The Effect of Esketamine Combined With Pregabalin on Chronic Postsurgical Pain in Patients After Craniotomy.
Chronic Postsurgical Pain
About this trial
This is an interventional treatment trial for Chronic Postsurgical Pain focused on measuring Esketamine, Pregabalin, Craniotomy, Chronic Postsurgical Pain
Eligibility Criteria
Inclusion Criteria:
- Adults, age ≥18 years, male or female
- American Society of Anaesthesiology (ASA) status I-III
- Patients undergoing elective craniotomy
Exclusion Criteria:
- Patients unable to complete scale assessment
- Pregnant or lactating women
- Patients with preoperative chronic pain syndrome
- Patients with previous craniotomy history
- Patients with a history of mental illness who are receiving medication
- Patients with liver and kidney dysfunction
- Patients have taken pain medication within two weeks
- Patients with history of adverse reactions to pregabalin, ketamine and esticketamine
- Patients with history of drug abuse;
- BMI>35.0 kg · m - 2.
Sites / Locations
- Beijing Tiantan Hospital, Capital Medical UniversityRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
Placebo Comparator
S-ketamine and pregabalin
Normal saline and placebo capsule
Drug: S-ketamine and pregabalin Drug: Pregabalin 150mg (2hrs) pre operatively and 75mg twice daily post operatively for 7 days(POD1-7),followed by dose reduction to 75mg once daily for 7days(POD8-14) Drug: S-ketamine infusion 0.5 mg/kg bolus after induction of anesthesia +0.12 mg/kg/h continuous intravenous infusion for 48 h
Drug: Normal saline and placebo capsule Drug: Placebo capsules :Two placebo capsules(2hrs) preoperatively and twice daily post operatively for 7days, followed by dose reduction to single capsule once daily for 7days Drug: Normal saline• 0.9% saline bolus after induction of anesthesia +intravenous infusion for 48 hours