Randomized double-blind controlled trial of patient-controlled epidural analgesia after gynecological abdominal surgery with levobupivacaine 0.125% or ropivacaine 0.2%
Not Applicable
- Conditions
- postoperative pain
- Registration Number
- JPRN-UMIN000026931
- Lead Sponsor
- Toho University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- Female
- Target Recruitment
- 120
Inclusion Criteria
Not provided
Exclusion Criteria
1.Malignant tumor surgery 2.Cesarean section 3.Allergy of the amide-type local anesthetic 4.Contraindication of the epidural anaesthesia 5.History of the neurologic disease 6.Treatment of choronic pain 7.Poorly understand usage of PCEA
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method