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Influence of the epidural labor analgesia on delivery outcomes and the analysis of related factors

Influence of the epidural labor analgesia on delivery outcomes and the analysis of related factors

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100044947
Enrollment
Unknown
Registered
2021-04-02
Start date
2019-01-01
Completion date
Unknown
Last updated
2021-11-02

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 vs non labor analgesia group:labor analgesia

Sponsors

Shandong Province Maternal and Child Health Care Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 34 Years

Inclusion criteria

Inclusion criteria: ASA II; Aged 20 to 34 years; weight 60-85kg; Singleton pregnancy; nulliparous women; Gestational age 38-41 weeks; Willing and able to provide consent.

Exclusion criteria

Exclusion criteria: Scarred uterus; obstetric complications,including hypertensive disorders of pregnancy, HELLP, antepartum haemorrhage; History of neuropsychiatric diseases; Contraindications of spinal anesthesia; Estimated neonatal weight >=4000g.

Design outcomes

Primary

MeasureTime frame
rate of cesarean section;labor duration;

Countries

China

Contacts

Public ContactLuo Shuzhi

Shandong Province Maternal and Child Health Care Hospital

luo666shuzhi@163.com+86 13853166612

Outcome results

None listed

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