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Fu Qingzhu's Bao Chan Wu You Fang for caesarean section due to cephalic dystocia: a randomized controlled trial

Fu Qingzhu's Bao Chan Wu You Fang for caesarean section due to cephalic dystocia: a randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-15007309
Enrollment
Unknown
Registered
2015-10-30
Start date
2015-11-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

cephalic dystocia

Interventions

intervention group:oral Fu Qingzhu's Bao Chan Wu You Fang
control group:none

Sponsors

Xiamen Hospital of Traditional Chinese Medicine Affiliated to Fujian University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Hospitalized gravidas meeting all the 5 criteria together as followings: (1) pregnancy at term, single birth, primiparity, and cephalic presentation; (2) a cephalopevic scoring 6scores; (3) prefer vaginal delivery; (4) agree to receive oral Bao Chan Wu You Fang; (5) volunteer to participate in this trial and gave written informed consent.

Exclusion criteria

Exclusion criteria: any of the followings: (1) unfit for vaginal delivery for indication of cesarean section; (2) with cardiovascular, cerebrovascular, liver, kidney, or hematopoietic disorders, or other serious diseases; (3) with preeclampsia need magnesium sulfate treatment or sedatives; (4) fetal hydrops hinted by ultrasound; (5) with mental illness; (6) poor compliance considered by investigators.

Design outcomes

Primary

MeasureTime frame
Proportion of caesarean section;

Secondary

MeasureTime frame
Proportion of dystocia;constuent ratio of delivery methods;postpartum blood lose;ratio of laceration of birth canal;ratio of fetal distress;ratio and constuent ratio of neonatal asphyxia;

Countries

China

Contacts

Public ContactTong Meihe
511941775@qq.com+86 13365928718

Outcome results

None listed

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