Investigation of the optimum rate of patient controlled epidural analgesia after cesarean sectio
Not Applicable
- Conditions
- Cesarean section
- Registration Number
- JPRN-UMIN000009939
- Lead Sponsor
- Asahikawa Medical University
- Brief Summary
The study has been terminated due to lack of participant.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- Female
- Target Recruitment
- 27
Inclusion Criteria
Not provided
Exclusion Criteria
Ptient refusal; known fetal anomalies; contraindication for combined spinal-epidural anesthesia because of hemodynamic, infectious, hemostatic, or neurological problems; severe preeclampsia; contraindication for the drugs used in the protocol; or failure of combined spinal-epidural anesthesia
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Degree of postcesarean analgesia
- Secondary Outcome Measures
Name Time Method