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The impact of epidural labor analgesia on Maternal and Infant Outcomes (Retrospective Study+Prospective Study)

The impact of epidural labor analgesia on Maternal and Infant Outcomes

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400088744
Enrollment
Unknown
Registered
2024-08-26
Start date
2024-08-30
Completion date
Unknown
Last updated
2024-09-02

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

Conditions

labor analgesia

Interventions

Labor analgesia:None
Control group (Normal natural delivery):None
Adverse Events Group for Labor Analgesia:none
Delivery analgesia without adverse events group:none

Sponsors

The Third Affiliated Hospital of Zhengzhou University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: Full term pregnancy (gestational age = 37 weeks) with a desire for vaginal delivery, ASA classification: Level I or II Level III, who voluntarily participate in the study and sign an informed consent form

Exclusion criteria

Exclusion criteria: There are contraindications for spinal anesthesia, a history of alcohol or substance abuse, a history of mental illness, or serious pregnancy complications.

Design outcomes

Primary

MeasureTime frame
Maternal adverse events;Fetal distress;Neonatal asphyxia;—

Secondary

MeasureTime frame
Maternal fever;postpartum hemorrhage;Respiratory depression;nausea and vomiting;itch;Neonatal hyperbilirubinemia;Neonatal infection;Transfer of parturient to cesarean section;Postpartum depression;Postpartum infection rate;—

Countries

China

Contacts

Public ContactWei Xiaoyong

The Third Affiliated Hospital of Zhengzhou University

38774209@qq.com+86 130 8366 5959

Outcome results

None listed

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