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Clinical analysis and risk factors of conversion from vaginal trial labor to cesarean section

Clinical analysis and risk factors of conversion from vaginal trial labor to cesarean section

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300077179
Enrollment
Unknown
Registered
2023-11-01
Start date
2023-11-01
Completion date
Unknown
Last updated
2023-11-06

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

Conditions

Delivery

Interventions

Observation group:None
Control group:None

Sponsors

Shanghai Sixth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: (1) 37 weeks=Gestational age<42 weeks (2) single birth, (3) first presentation, (4) pregnant women who have the intention of vaginal trial labor and can perform vaginal trial labor after evaluation by senior asset department physicians during labor, and (5) complete case data records.

Exclusion criteria

Exclusion criteria: (1) Gestational age 42 weeks, (2) obvious head basin asymmetry, (3) abnormal fetal position, including breech and transverse position, (4) patients who cannot perform trial labor due to serious medical and surgical diseases, (5) patients with incomplete medical records, (6) patients with cicatricial uterus, (7) patients with forceps or fetal head aspiration assisted delivery.

Design outcomes

Primary

MeasureTime frame
cesarean section rate;

Secondary

MeasureTime frame
Indicationgs for cesarean section;Risk factors of cesarean section;Maternal and infant outcome;

Countries

China

Contacts

Public ContactLiu Xinying

Shanghai Sixth People's Hospital

1129835902@qq.com+86 166 2117 5569

Outcome results

None listed

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