The application of wireless temperature sensor in epidural labor analgesia puerpera

Effect of different cooling measures after intrapartum fever during epidural labor analgesia on delivery outcome and newborn

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2100045871

Enrollment

Unknown

Registered

2021-04-25

Start date

2021-07-01

Completion date

Unknown

Last updated

2021-12-13

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

Conditions

epidural-related maternalfeve

Interventions

Fever group:1. Physical cooling

2. Oral antipyretics

3. No intervention.

No fever group:Nil

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: Expectant mothers proposed by vaginal delivery and implemented epidural labor analgesia.

Exclusion criteria

Exclusion criteria: 1. Suffer from autoimmune diseases; 2. Take a lot of steroids during pregnancy and before delivery; 3. Pregnant women whose pregnancy is diagnosed as sepsis, meningitis, pneumonia, congenital infection or viral infection; 4. If during labor, due to changes in medical conditions, women who switch to cesarean section before the start of labor analgesia.

Design outcomes

Primary

Measure	Time frame
Maternal body temperature;	—

Countries

China

Contacts

Public ContactSun Jianliang

The First People's Hospital of HangZhou

jxmzsjl@163.com+86 13958069878

Outcome results

None listed

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