Comparison of the analgesic effect of magnesium and Tramadol after local anesthesia of upper extremity.
Not Applicable
- Conditions
- Acute Postoperative Pain.Acute pain
- Registration Number
- IRCT2014040511662N6
- Lead Sponsor
- Vice-Chancellery of Research and Technology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 69
Inclusion Criteria
69 patients 15-65 years old with ASA 1&2candidates for elective hand and forearm surgery or due to trauma.
Exclusion criteria: History of drug abuse; History of allergies to drugs such as local anesthetics or opioid; History of: liver diseases; cardiovascular disease; renal failure; sickle cell anemia; Raynaud's disease; coagulopathy; G6PD deficiency; seizures.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Postoperative pain intensity. Timepoint: Every hour for 6 hours and then every 4 hours for 24 hours after surgery. Method of measurement: Visual Anlouge Scale.
- Secondary Outcome Measures
Name Time Method ausea and Vomiting. Timepoint: Every one hour during first postoperative 24 hr. Method of measurement: Nausea is defined as urge to vomiting without ejection ofof the contents of the stomach through the mouth, Vomiting is defined asto eject of the contents of the stomach through the mouth, usually in a series of involuntary spasmic movements.