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NCT07175363

Butorphanol for Pain Relief After Cesarean Section: A Retrospective Study

Sponsor: Sichuan Provincial People's Hospital

View on ClinicalTrials.gov

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 duration, etc.) by retrospectively analyzing the clinical data of patients undergoing cesarean section in the main campus and branches of Sichuan Provincial People's Hospital from September 2024 to June 2025. The value of this study lies in: 1) providing a basis for optimizing the postoperative analgesia plan after cesarean section. 2) To provide references for the formulation of personalized analgesia strategies in clinical practice, improve the postoperative recovery quality of patients, promote the concept of enhanced recovery after surgery, and reduce the medical burden.

Official title: The Application of Butorphanol in Postoperative Analgesia Management After Cesarean Section: A Retrospective Cohort Study

Key Details

Gender

FEMALE

Age Range

18 Years - 55 Years

Study Type

OBSERVATIONAL

Enrollment

2500

Start Date

2025-09-20

Completion Date

2026-06-30

Last Updated

2025-09-16

Healthy Volunteers

No

Interventions

DRUG

An postoperative analgesic pump was used

The drugs in the analgesic pump include butorphanol, hydromorphone, tramadol, and other medications.