The effect of lidocaine and ketamine on pain after upper limb orthopedic surgery
Phase 3
- Conditions
- pper extremity orthopedic surgery.
- Registration Number
- IRCT20200825048515N68
- Lead Sponsor
- Esfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 180
Inclusion Criteria
Candidate patients for elective upper extremity orthopedic surgery under general anesthesia
Age 65-18 years
Informed consent to participate in this study
Exclusion Criteria
Addiction to opioid products
Having an underlying disease (hypertension and uncontrolled diabetes or any neurological disorder) that has led to impaired sensation or movement of the operated organ
Hypersensitivity to lidocaine or ketamine
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Mean arterial pressure. Timepoint: In the basic times, the first hour every 15 minutes, the second hour every 30 minutes, the next 4 hours every 1 hour and after that every 2 hours for 24 hours. Method of measurement: Monitoring device.;Heart beat. Timepoint: In the basic times, the first hour every 15 minutes, the second hour every 30 minutes, the next 4 hours every 1 hour and after that every 2 hours for 24 hours. Method of measurement: Monitoring device.;Oxygen saturation percentage (SPO2). Timepoint: In the basic times, the first hour every 15 minutes, the second hour every 30 minutes, the next 4 hours every 1 hour and after that every 2 hours for 24 hours. Method of measurement: Monitoring device.;Pain. Timepoint: In the basic times, the first hour every 15 minutes, the second hour every 30 minutes, the next 4 hours every 1 hour and after that every 2 hours for 24 hours. Method of measurement: Visual Analogue Scale (VAS).
- Secondary Outcome Measures
Name Time Method