Effect of Naloxane and/or Opioids on Supraclavicular Block
Not Applicable
- Conditions
- Pain.acute pain
- Registration Number
- IRCT201209175140N6
- Lead Sponsor
- Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
Inclusion Criteria: Patients with American Society of Anesthesiologists physical status class I and II.
Exclusion Criteria
Hepatic or Renal failure; Heart diseases; history of drug allergy; substance abuse (including opioids and benzodiazepines); morbid obesity; history of postoperative nausea and vomiting (PONV); history of motion sickness; smokers.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Sensory block Onset time and duration. Timepoint: Every 5 minutes from supraclavicular block. Method of measurement: measurement of time.;Motor block onset and duration time. Timepoint: Time from supraclavicular block, every 5 minutes. Method of measurement: measurement of time.
- Secondary Outcome Measures
Name Time Method Pruritus. Timepoint: Time from supraclavicular block, every 5 minutes. Method of measurement: measurement of time.