Status:
NOT_YET_RECRUITING
Butorphanol for Pain Relief After Cesarean Section: A Retrospective Study
Lead Sponsor:
Sichuan Provincial People's Hospital
Conditions:
Caesarean Section
Eligibility:
FEMALE
18-55 years
Brief Summary
This study explored the association between postoperative functional recovery and the formula of analgesic pumps as well as other related factors (such as age, intraoperative blood loss, operation dur...
Eligibility Criteria
Inclusion
- Age 18-55 years
- ASAI-III level
- Scheduled or emergency cesarean section
- Postoperative use of analgesic pump (formulation includes buprenorphine or tramadol or hydromorphone, etc.)
- Complete electronic medical records
Exclusion
- Postoperative analgesia pump usage time is less than 24 hours
- Missing key information such as follow-up status in medical records
Key Trial Info
Start Date :
September 20 2025
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
June 30 2026
Estimated Enrollment :
2500 Patients enrolled
Trial Details
Trial ID
NCT07175363
Start Date
September 20 2025
End Date
June 30 2026
Last Update
September 16 2025
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