Study on the rate of motor block and postoperative pain in patients undergoing shoulder surgery..
Conditions
Interventions
Intervention 1: First Intervention group: Received dexmedetomidine 5mcg/kg with 30cc ropivacaine 0.5% perineural. Intervention 2: Second Intervention group: Received dexmedetomidine 5mcg/kg intravenou
Sponsors
Tehran University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 75 Years
Inclusion criteria
Inclusion criteria: Patients age between 18 to 75 years old Patients undergoing elective shoulder surgery Patients with ASA class one and two
Exclusion criteria
Exclusion criteria: Known Allergy to local anesthetic drugs Presence any kinds of neurologic, vascular and neuromuscular diseases Presence of hematologic and coagulation abnormalities Chronic opioid usage (more than six months)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Duration of Interscalen block. Timepoint: The duration of sensory block is determined from the onset of the block (confirmed by pinprick testing) until the return of sensation. The duration of motor block is determined from the onset of the block (confirmed by loss of muscle force) until the return of full force. Method of measurement: The variables are based on sensory clinical examination (pinprick test) and motor clinical examination (muscle force test). | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactHamed Abdollahi
Tehran University of Medical Sciences
Outcome results
None listed