A double-blind randomized comparison in the analgesic efficacy between programmed intermittent epidural bolus (PIEB) and continuous epidural infusion (CEI) in patients undergoing cesarean section.
Not Applicable
Active, not recruiting
- Conditions
- Pregnancy, childbirth and the puerperium
- Registration Number
- KCT0004203
- Lead Sponsor
- Jeju National University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Active, not recruiting
- Sex
- Female
- Target Recruitment
- 90
Inclusion Criteria
healthy (ASA physical status I or II), term (>36 gestation weeks) parturients, who scheduled cesarean section under combined spinal epidural (CSE) anesthesia
Exclusion Criteria
with contraindications to neuraxial blockade or narcotics, history of drug abuse, severe systemic disease (e.g., eclampsia, severe asthma, cardiac, liver or renal disease), or emergency operation were excluded.
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method delivered PCEA boluses
- Secondary Outcome Measures
Name Time Method rescue analgesics;pain visual analog score (VAS);side effects related to epidural analgesic (nausea, vomiting, pruritus, paresthesia, motor disturbance)