Forearm surgery. Unspecified fracture of forearm
Conditions
Interventions
Intervention 1: Intervention group: The first group 3 mg/kg lidocaine 0.5% diluted with 0.9% normal saline at a total volume of 40 cc. Intervention 2: Intervention group: The second group 3 mg/kg l
Sponsors
Bandare-abbas University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 50 Years
Inclusion criteria
Inclusion criteria: All Candidates aged 18-50 years for- forearm surgery with ASA I,II classes
Exclusion criteria
Exclusion criteria: Patients who are allergic to sufentanil or topical anesthetic. Patients with a history of liver or kidney disease. Patients who have sickle cell anemia or convulsion. Patients with Raynaud syndrome and neuropathy. Patients who have uncontrolled hypertension and opioid addiction.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Tourniquet pain. Timepoint: Pain intensity measurement at baseline (before intervention) and 5,10,15 and 20 min after injection. Method of measurement: Patients' severity of pain is based on the Visual Analogues Scale.;Quality of local anesthesia. Timepoint: During Surgery. Method of measurement: Numerical scale(1-4) of patient satisfaction. | — |
Secondary
| Measure | Time frame |
|---|---|
| The evaluation of sensory block. Timepoint: During surgery every 10 minutes. Method of measurement: 22-gauge needle on palm in hypothenar (ulna nerve) and thenar (median nerve) eminences and back of the upper arm between thumb and forefinger (radial nerve).;The evaluation of motor block. Timepoint: During surgery every 10 minutes. Method of measurement: Observation.;Side effects such as nausea, vomiting, seizures, hypotension, bradycardia, and itching. Timepoint: During and after surgery. Method of measurement: Observation. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactHashem Jarineshin
Bandare-abbas University of Medical Sciences
Outcome results
None listed