Comparison of the effects of local anesthetics on the severity of pain after cesarean sectio
Phase 2
- Conditions
- Anesthesia and delivery.Complications of anaesthesia during labour and delivery
- Registration Number
- IRCT2015090723926N1
- Lead Sponsor
- Vice chancellor for research, Babol University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 160
Inclusion Criteria
Term Pregnancy; single pregnancy; ASA class I or II; Height 180 to 170 cm,; End pregnancy weight from 100 to 70 kg and undergoing elective cesarean section.
Exclusion criteria: having hypersensitivity to amide local anesthetics (eg, bupivacaine and lidocaine), magnesium sulfate and epinephrine; history of opioid drugs; coagulopathy; seizure; cardiovascular disease; mental disorders; asthma and chronic obstructive pulmonary disease; high ICP; kidney disease; liver disease; atrioventricular block; history of calcium channel blockers; A tonic uterus after surgery or prolong surgical time more than 1.5 hours
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Severity of pain. Timepoint: 2, 6, 12, 18 and 24 hours after after starting the intervention. Method of measurement: visual Analogous Scale of pain.
- Secondary Outcome Measures
Name Time Method Blood pressure. Timepoint: 2, 6, 12, 18 and 24 hours after starting intervention. Method of measurement: Observation and record.;Heart rate. Timepoint: 2, 6, 12, 18 and 24 hours after starting intervention. Method of measurement: Observation and record.