Supraclavicular Blochade of the Brachial Plexus.
Conditions
Interventions
Intervention 1: Supraclavicular injection of 30ml Bupivacaine 0.5% + Administration of 25mcg/kg/min IV Propofol. Intervention 2: Supraclavicular injection of 20ml Bupivacaine 0.5% + Administration of
Treatment - Drugs
Supraclavicular injection of 30ml Bupivacaine 0.5% + Administration of 25mcg/kg/min IV Propofol
Supraclavicular injection of 20ml Bupivacaine 0.5% + Administration of 25mcg/kg/min IV Propofol
Supraclavicular injection of 30ml Bupivacaine 0.5% + Administration of 25mcg/kg/min IV normal saline as placebo
Sponsors
Tehran University of Medical Sciences, The Vice-Chancellery for Research
Eligibility
Sex/Gender
All
Age
20 Years to 50 Years
Inclusion criteria
Inclusion criteria: Inclusion Criteria: Ages between 20 and 50; ASA classes: I,II,III; BMI under 35; Absence of the history of drug induced hypersensitivity; Taking of informed consent Exclusion Criteria: Failure of supraclavicular blockade; Need to General Anesthesia
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Duration of Motor Blockage. Timepoint: During and after the intervention. Method of measurement: Physical examination by the physician.;Duration of Sensory Blockage. Timepoint: During and after the intervention. Method of measurement: Physical examination by the physician.;Onset of the Motor Blockage. Timepoint: During the intervention. Method of measurement: Physical examination by the physician.;Onset of the Sensory Blockage. Timepoint: During the intervention. Method of measurement: Physical examination by the physician. | — |
Secondary
| Measure | Time frame |
|---|---|
| Patient's feeling of pain. Timepoint: After the intervention in the same admission. Method of measurement: Visual Analogue Scale (VAS).;The measure of motor blockade. Timepoint: During and after the intervention. Method of measurement: Lovett Rating Scale.;The time of the first opioid request by the patient. Timepoint: After the intervention in the same admission. Method of measurement: By using PCA(Patient Controlled Anaesthesia).;Administered opioid dosage in 24 hours. Timepoint: After the intervention in the same admission. Method of measurement: Patient Medical Document.;Duration of the surgery. Timepoint: During the intervention. Method of measurement: Patient Medical Document.;Nausea and vomiting after the surgery. Timepoint: After the intervention in the same admission. Method of measurement: Asking the patient.;Mean arterial blood pressure 1 minute after the blockade. Timepoint: 1 minute after the blockade. Method of measurement: Non-invasive automatic manometer.;Mean arterial blood pressure 3 minutes after the blockade. Timepoint: 3 minutes after the blockade. Method of measurement: Non-invasive automatic manometer.;Mean arterial blood pressure 5 minutes after the blockade. Timepoint: 5 minutes after the blockade. Method of measurement: Non-invasive automatic manometer.;Mean arterial blood pressure 1 minute after the recovery. Timepoint: 1 minute after recovery admission. Method of measurement: Non-invasive automatic manometer.;Mean arterial blood pressure 3 minutes after the recovery. Timepoint: 3 minutes after the recovery admission. Method of measurement: Non-invasive automatic manometer.;Mean arterial blood pressure 5 minutes after the recovery. Timepoint: 5 minutes after the recovery admission. Method of measurement: Non-invasive automatic manometer.;Heart rate 1 minute after the blockade. Timepoint: 1 minute after the blockade. Method of measurement: Pulse Oxymetery.;Heart rate 3 minutes after the blockade. Timepoint: 3 minutes after the blockade. Met | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMehrdad Sadri
Tehran University of Medical Sciences, School of Medicine
Outcome results
None listed