The effect of ultra-low dose of naloxone on analgesia after abdominal wall nerves block in patients after cesarean sectio
Not Applicable
- Conditions
- pain.acute pain
- Registration Number
- IRCT2013041212958N2
- Lead Sponsor
- Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 164
Inclusion Criteria
inclusion criteria:
age 20-40; ASA class I,II; primigravid; non addict; without history of allergy to protocol drugs
Excluxion criteria:
patients whom recieved drugs other than the ones mentioned in protocol in 24 h preoperation; surgery duration more than 90 minutes
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain intesity. Timepoint: recovery room,2,6,12,24 h after surgery. Method of measurement: visual analoge scale.;Morphine consumption. Timepoint: recovery room, 2,6,12,24h after surgery. Method of measurement: opioid registration by milligram.
- Secondary Outcome Measures
Name Time Method Sensory Block Duration. Timepoint: 24h. Method of measurement: Pinprick test.