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A multi-center randomized, double-blind trial studying the effect of flurbiprofen with epidural analgesia on the wound pain and uterine cramping pain after cesarean section

A multi-center randomized, double-blind trial studying the effect of flurbiprofen with epidural analgesia on the wound pain and uterine cramping pain after cesarean section

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-17011956
Enrollment
Unknown
Registered
2017-07-12
Start date
2017-07-17
Completion date
Unknown
Last updated
2017-07-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

cesarean section

Interventions

epidural group:no
flurbiprofen+epidural analgesia group:iv flurbiprofen

Sponsors

Guangzhou Women and Children's Medical Center
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: ASA physical status I–II term parturients (37–42 wk gestational age); Age between 18 and 45 years; The time of cesarean delivery under spinal anesthesia is from 8am to 12am; BMI 18 to 35.

Exclusion criteria

Exclusion criteria: contraindication to spinal anesthesia; known hypersensitivity or intolerance to study drugs;medical disorders like asthma, gastric ulcers, abnormal liver or renal function, disorders of hematopoiesis, diabetes, mental disorders; severe preeclampsia; bleeding tendency; concomitant use of other analgesics in the past 24 hours; refusal to use, or poor adherence to PCEA.

Design outcomes

Primary

MeasureTime frame
pain scores;

Secondary

MeasureTime frame
Rasmay sedation scores;the doses of analgesic drugs;EPDS score;

Countries

China

Contacts

Public ContactSong Xingrong

Guangzhou Women and Children's Medical Center

songxr1966@yeah.net+86 13922416303

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026