Pain relief after tibial fracture surgery. Acute pain
Conditions
Interventions
Intervention 1: Patient s in control group received normal saline IV infusion. Intervention 2: Patients in intervention group received lidocaine (lidocaine group) with a 1.5 mg/kg intravenous bolus an
Placebo
Prevention
Patient s in control group received normal saline IV infusion
Patients in intervention group received lidocaine (lidocaine group) with a 1.5 mg/kg intravenous bolus and followed by a 1.5 mg . kg intravenous infusion
Sponsors
Ahvaz Jundishapur University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 50 Years
Inclusion criteria
Inclusion criteria: Inclusion Criteria: patients undergoing tibial fracture surgery under general anesthesia; age 18-50inclusive; ASA class I patients ; Body Mass Index (BMI) of 18.5-35 (Includes 18.5 to 25 – healthy range; >25-30 overweight; >30-35 Obese Class I); Exclusion Criteria: patients under age 18 or over age50; ASA,II III, IV and V class patients ; Obese Class II patients (BMI>35) or undernourished (BMI<18.5); history of Liver dysfunction ; renal insufficiency; history of seizure disorder; hypersensitivity or allergy to amide type local anesthetics; medication use(daily use of any opiods or analgesic) and any chronic pain syndromes ;
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pethedine consumpsion. Timepoint: 1, 2, 4, 12 , 16 , 20 and 24 hours post extubation. Method of measurement: Medical records. | — |
Secondary
| Measure | Time frame |
|---|---|
| Pain. Timepoint: 1, 2, 4, 12 , 16 , 20 and 24 hours after extubation. Method of measurement: Visual analog scale (VAS). | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr. Sholeh Nesioonpour
Ahvaz Jundishapur University of Medical Sciences
Outcome results
None listed