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Early identification of histological chorioamnionitis by routine blood parameters in parturients with intrapartum fever

An investigation of the change of maternal fever during interpartum before and after delivery

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100053554
Enrollment
Unknown
Registered
2021-11-24
Start date
2021-12-01
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

intrapartum fever

Interventions

Control group (without HCA):None
Observation group (with HCA combined):None

Sponsors

Nanjing Maternal and Child Health Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Singleton full-term pregnant women with body temperature >= 38? who were treated with epidural labor analgesia, with complete clinical data, underwent blood routine examination within 2 hours of fever, and placenta pathological examination after delivery.

Exclusion criteria

Exclusion criteria: 1. Diagnosed with clinical chorioamnionitis; 2. Complicated with various acute and chronic infections, premature rupture of membranes and other serious medical and surgical diseases upon admission; 3. Those who have been treated with antibiotics and non-steroidal anti-inflammatory drugs within 1 week before admission.

Design outcomes

Primary

MeasureTime frame
Blood routine;Pathological examination of placenta;Temperature;—

Countries

China

Contacts

Public ContactFan Yuru

Nanjing Maternal and Child Health Hospital

fyr1899@njmu.edu.cn+86 18606190360

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 10, 2026