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A risk score system for maternal intrapartum fever and the potential adverse perinatal effects induced by fever after combined spinal-epidural labor analgesia during vaginal delivery

A risk score system for maternal intrapartum fever and the potential adverse perinatal effects induced by fever after combined spinal-epidural labor analgesia during vaginal delivery

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900021715
Enrollment
Unknown
Registered
2019-03-05
Start date
2019-03-01
Completion date
Unknown
Last updated
2021-01-18

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

Conditions

Intrapartum fever

Interventions

Development group:None
Validation group:None

Sponsors

Third Affiliated Hospital of Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
17 Years to 42 Years

Inclusion criteria

Inclusion criteria: 1. Patients voluntarily participate in this study and sign an informed consent form; 2. Healthy,singleton pregnant women who will get combined spinal-epidural labor analgesia.

Exclusion criteria

Exclusion criteria: 1. Patients who have colds or fevers ( >= 38 degrees C) or with infectious diseases. 2. Patients use antibiotics or antipyretic or NSAID or glucocorticoids within 24 hours before CSE. 3. Patients who have accidental dural puncture. 4. Patients with total stage of labor less than three hours or induction of labor in the second trimester. 5. Patients who are allergic to ropivacaine or sufentanil.

Design outcomes

Primary

MeasureTime frame
Incidence of intrapartum fever;Delivery-related data;—

Secondary

MeasureTime frame
Score for VAS;Uncomfortable feeling after analgesia;Uncomfortable feeling after analgesia;intrapartum and CSE-procedural data;Demographic obstetric data;Length of labor stage;—

Countries

China

Contacts

Public ContactDezhao Liu

Third Affiliated Hospital of Sun Yat-sen University

sumsldz@126.com+86 15360884591

Outcome results

None listed

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