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Influence of epidural labor analgesia on labor outcomes in women with a total labor duration of more than 24 hours under the new labor process management model

Influence of epidural labor analgesia on labor outcomes in women with a total labor duration of more than 24 hours under the new labor process management model - a single-center, retrospective cohort study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000037601
Enrollment
Unknown
Registered
2020-08-29
Start date
2020-09-01
Completion date
Unknown
Last updated
2020-11-02

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

Conditions

labor analgesia

Interventions

epidural labor analgesia group :Nil
without labor analgesia group:Nil

Sponsors

Shenzhen Maternal and Child Health Care Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 48 Years

Inclusion criteria

Inclusion criteria: (1) Full-term delivery; (2) Single pregnancy; (3) cephalic presentation; (4) Vaginal trial delivery can be evaluated by the obstetrician; (5) Live birth; (6) The total labor time is more than 24 hours.

Exclusion criteria

Exclusion criteria: (1) The opening of the uterus before entering the delivery room or the mother has given birth; (2) Severe pregnancy complications or pregnancy complications (severe preeclampsia, pregnancy with severe heart disease, etc.); (3) Known fetal distress or major fetal malformations and chromosomal abnormalities and direct surgical delivery without a vaginal trial.

Design outcomes

Primary

MeasureTime frame
labor outcome;Cesarean section rate;—

Countries

China

Contacts

Public ContactLi Yuantao

Shenzhen Maternal and Child Health Care Hospital

szmchlyt@smuedu.cn+86 15013857589

Outcome results

None listed

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