Forearm bones fracture. Fracture of radius or ulna following insertion of orthopedic implant, joint prosthesis, or bone plate
Conditions
Interventions
Intervention 1: Intervention group: Patients in the intervention group one receive 24 ml of bupivacaine(bupivacaine,Mylan,A.S.A, France)( 0.5%) plus 1 ml of dexamethasone (4 mg)(Caspian, Iran) for s
Sponsors
Shiraz University of Medical Sciences
Eligibility
Sex/Gender
All
Age
21 Years to 60 Years
Inclusion criteria
Inclusion criteria: Age 21 to 60 years old Fractures of the forearm surgeries under supraclavicular plexus block
Exclusion criteria
Exclusion criteria: Heart disease Patients with high blood pressure Bradycardia Hyperthyroidism Cardiac Blocks of Grade 1,2,3 Use of adrenoreceptor agonist and antagonist Peripheral neuropathy pregnant women Patients who are addicted to narcotics and stimulant drugs Patients susceptible or allergic to the drugs studied Coagulation disorders Local infections Patient refusal
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Duration of sensory block. Timepoint: 15 and 30 minutes after entering the recovery and 1,2,4,6,12,18,24 in the ward. Method of measurement: pinprick.;Onset of the sensory block. Timepoint: At 0.1, 5. 10, 15, 20, 25 and 30 min after the injection of anesthetics. Method of measurement: pinprick.;Duration of the motor block. Timepoint: 15 and 30 minutes after entering the recovery and 1,2,4,6,12,18,24 in the ward. Method of measurement: Bromage.;Onset of the motor block. Timepoint: 15 and 30 minutes after entering the recovery and 1,2,4,6,12,18,24 in the ward. Method of measurement: Bromage. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactIsaa Ahmadizadeh
Shiraz University of Medical Sciences
Outcome results
None listed