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The mechanism of labor intraspinal analgesia with intrapartum fever

The mechanism of labor intraspinal analgesia with intrapartum fever

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200059293
Enrollment
Unknown
Registered
2022-04-28
Start date
2022-04-29
Completion date
Unknown
Last updated
2024-02-26

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

Conditions

intrapartum fever

Interventions

group 1:None
group 2:Patient-controlled epidural analgesia
group 3 :Patient-controlled epidural analgesia

Sponsors

People's Hospital of Yantian District, Shenzhen
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1. Aged >=18 years old, 37 to 42 weeks pregnant; 2. Primiparas with single and head position; 3. Patients with ASA grades I or II; 4. Patients who voluntarily request labor analgesia or unwilling to do so.

Exclusion criteria

Exclusion criteria: 1. Have used opioids or sedatives within 4 hours before epidural puncture, and have a history of drug abuse; 2. Premature rupture of membranes more than 6 hours during analgesia; 3. Those with body temperature>37.5 ? before analgesia; 4. GBS (+) in combination with other systemic infections; 5. Contraindications of epidural analgesia; 6. Morbid obesity; 7. There are pregnancy complications, such as diabetes in pregnancy, pregnancy hypertension, heart disease in pregnancy, pre eclampsia, placenta previa, etc.

Design outcomes

Primary

MeasureTime frame
RNA-seq;star factor of RNA-seq;

Secondary

MeasureTime frame
VAS score;

Countries

China

Contacts

Public ContactHongyan Huang

People's hospital of Yantian District,Shenzhen

hhy1129@sina.cn+86 13682347360

Outcome results

None listed

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