External cephalic version success rate and influencing factorsbased on the prospective clinical study

External cephalic version success rate and influencing factors based on the prospective clinical study

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR1900027062

Enrollment

Unknown

Registered

2019-10-30

Start date

2019-11-01

Completion date

Unknown

Last updated

2022-01-24

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

Conditions

breech presentation

Interventions

success group and failure group:External cephalic versio

Eligibility

Sex/Gender

Female

Age

18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Single pregnancy, 32~37+6 weeks of pregnancy confirmed by ultrasound as breech presentation, amniotic fluid index was normal, there was no indication of absolute cesarean section, and there were vaginal trial delivery volunteers.

Exclusion criteria

Exclusion criteria: Severe uterine malformation, multiple pregnancies, premature rupture of membranes, antenatal bleeding, abnormal fetal supervision or indication of absolute cesarean section.

Design outcomes

Primary

Measure	Time frame
External cephalic version success rate;	—

Countries

China

Contacts

Public ContactZhou Ye

The International Peace Maternity & Child Health Hospital of China welfare institute (IPMCH)

13916232488@163.com+86 021-64070434

Outcome results

None listed

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