Evaluation the effect of dexmedetomidine with bupivacaine on postoperative pai
Phase 2
- Conditions
- Pain.Generalized pain NOSR52.9
- Registration Number
- IRCT20160430027677N15
- Lead Sponsor
- Oroumia University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
Aged 20-60 years old
American Society of Anesthesiologists physical status classification I
General anesthesia
Exclusion Criteria
History of cardiovascular disease
History of respiratory disease
History of renal disease
History of liver disease
Pregnancy
Allergy to the drugs studied
Contraindication of supraclavicular block
Coagulopathy
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: In recovery, 6, 12 and 24 hours after surgery. Method of measurement: Visual Analogue Scale.;Duration of the sensory block. Timepoint: From the onset of the sensory block until the onset of the first pain after surgery. Method of measurement: Pinprick.;Duration of the motor block. Timepoint: Since full paralysis of limb until complete restoration of limb movement. Method of measurement: Bromage scale.
- Secondary Outcome Measures
Name Time Method Mean Arterial Blood Pressure. Timepoint: During surgery. Method of measurement: None Invasive Blood Pressure.;Mean pulse Rate. Timepoint: During surgery. Method of measurement: Electrocardiogram.;Pentazocine consumption. Timepoint: After transferring the patient to the ward in the first 24 hours. Method of measurement: milligram.