Regional anesthesia. Local anaesthetics
Conditions
Interventions
Intervention 1: Intervention group will take 3 mg/kg lidocaine 0.5% with 1 mg granisetron diluted to 40 cc saline 0.9% will infuse over 90 seconds. Intervention 2: Control group will take 3 mg/kg lido
Treatment - Drugs
Intervention group will take 3 mg/kg lidocaine 0.5% with 1 mg granisetron diluted to 40 cc saline 0.9% will infuse over 90 seconds.
Control group will take 3 mg/kg lidocaine 0.5% diluted to 40 cc saline 0.9% will infuse over 90 seconds.
Sponsors
Arak University of Medical Sciences, Vice chancellor for research
Eligibility
Sex/Gender
All
Age
20 Years to 50 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: age between 20 to 50 years old; ASA I or II. Exclusion criteria: history of drug allergy; pregnancy; contraindication of intravenous regional anesthesia like sickle cell anemia; use of opiate and analgesic drugs; use of Apomorphine.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Tourniquet pain. Timepoint: 0, 15, 30 and 45 minute after injection. Method of measurement: VAS. | — |
Secondary
| Measure | Time frame |
|---|---|
| Reduction of pain. Timepoint: Every 30 minutes until 2 hours after removing tourniquet. Method of measurement: VAS.;Vital signs. Timepoint: After removing tourniquet. Method of measurement: Physical examination.;O2 saturation. Timepoint: After removing tourniquet. Method of measurement: Pulse oxymeter.;Need to Fentanyl. Timepoint: 0, 15, 30 and 45 min after injection. Method of measurement: Drug dose that is used. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactHesameddin Modir
Vali-e-Asr hospital
Outcome results
None listed