Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
NCT06682416

The Impact of Local Anesthetic Solution Temperature on Epidural-related Maternal Fever

Led by The First Affiliated Hospital of Soochow University · Updated on 2025-09-11

424

Participants Needed

2

Research Sites

147 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study investigates how the temperature of local anesthetics affects maternal fever related to epidural analgesia during childbirth. The research is a prospective, randomized controlled trial involving 424 participants from two hospitals. The primary objective is to investigate the impact of local anesthetic solution temperature on intrapartum fever in parturients. Secondary goals include assessing the impact on the efficacy of epidural analgesia and various maternal and neonatal outcomes. Participants will receive either 37°C or 23°C anesthetic solutions, and data will be collected on fever rates, pain scores, and other health indicators. The study runs from January 2024 to December 2026.

CONDITIONS

Official Title

The Impact of Local Anesthetic Solution Temperature on Epidural-related Maternal Fever

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Requesting epidural analgesia
  • Aged 18 or older
  • At least 37 weeks of pregnancy
  • Planning vaginal delivery
Not Eligible

You will not qualify if you...

  • Contraindications to epidural analgesia
  • Fever of 386C or higher before labor
  • Use of NSAIDs or other fever-reducing drugs before labor
  • Multiple pregnancy (more than one fetus)
  • Fetal death before delivery
  • Severe preeclampsia
  • Refusal to participate in the study

AI-Screening

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Trial Site Locations

Total: 2 locations

1

Ethical Committee of the First Affiliated Hospital of Soochow University

Suzhou, Jiangsu, China, 215000

Actively Recruiting

2

Suzhou Municipal Hospital

Suzhou, Jiangsu, China

Not Yet Recruiting

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Research Team

D

Dapeng Chen

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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