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Risk factors analysis of transition from vaginal trial to cesarean section in women undergoing epidural analgesia during delivery: a single center retrospective study

Risk factors analysis of transition from vaginal trial to cesarean section in women undergoing epidural analgesia during delivery: a single center retrospective study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500098294
Enrollment
Unknown
Registered
2025-03-05
Start date
2025-03-05
Completion date
Unknown
Last updated
2025-03-10

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

Conditions

Pregnancy

Interventions

Obseravation group:None

Sponsors

The First Affiliated Hospital of Shan Tou University Medical College
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1.Primipara and metapara who underwent epidural labor analgesia in the obstetric department of our hospital during the study period; 2.Choose epidural labor analgesia voluntarily and sign an informed consent form; 3.Medical records and follow-up data were complete.

Exclusion criteria

Exclusion criteria: 1.Clinical information is missing, data are incomplete or inaccessible; 2.Stillbirth, miscarriage (e.g. epidural labor analgesia and abortion); 3.Complications such as analgesia failure, cauda equina syndrome and epidural hematoma occurred during the process of analgesia.

Design outcomes

Primary

MeasureTime frame
Caesarean section;—

Countries

China

Contacts

Public ContactZeting Qiu

The First Affiliated Hospital of Shantou University Medical College

doctorqiuzt@gmail.com+86 13580546462

Outcome results

None listed

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