idocaine with ketamine in posterior spine fusio
- Conditions
- Anaesthesia
- Registration Number
- PACTR202103785412583
- Lead Sponsor
- Mostafa Mansour Hussein
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 60
60 adult patients aged between 18 - 65 years old, undergoing elective two or more levels of lumbar posterior spine fusion under general anesthesia will be enrolled in this study. Inclusion criteria include patients of both genders with American Society of Anesthesiologists (ASA) physical status I/II.
Known hypersensitivity to lidocaine or ketamine, pregnancy, severe renal disorder, hepatic dysfunction, cardiac arrhythmias, severe cardiac or pulmonary disease, increased intraocular pressure, history of psychiatric disorders, epilepsy, history of alcohol or drug abuse, patients receiving beta-blockers or antiarrhythmics, uncontrolled diabetes or hypertension, and patients unable to operate patient-controlled analgesia (PCA) pump.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method