Skip to content

Effect of dexmedetomidine on intrapartum fever during epidural labor analgesia

Effect of dexmedetomidine on intrapartum fever during epidural labor analgesia

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900027861
Enrollment
Unknown
Registered
2019-11-30
Start date
2020-03-01
Completion date
Unknown
Last updated
2019-12-10

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

Conditions

Epidural-related maternal fever

Interventions

Simple ropivacaine group:Epidural administration of Ropivacaine alone
Ropivacaine combined with Sufentanil group:Epidural administration of Ropivacaine combined with Sufentanil
Ropivacaine combined with Dexmedetomidine group:Epidural administration of Ropivacaine combined with Dexmedetomidine

Sponsors

Affiliated Hospital of Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Suitable for vaginal delivery, voluntary labor analgesia,aged 20 ~ 35 years; 2. Gestation ranges from 37 to 41 weeks,singletons, cephalic presentation, height:150-175cm, weight:55-85kg; 3. ASAI-II?; 4. Normol fetal heart and movement.

Exclusion criteria

Exclusion criteria: 1. History of severe cardiopulmonary disease, bradycardia; 2. Morbid obesity, severe preeclampsia, macrosomia, multiple births, etc.; 3. History of cesarean section or induction of labor; 4. Contraindications for epidural analgesia; 5. Diabetes, hyperthyroidism, hypothyroidism and other metabolic diseases; 6. Basal body temperature >= 38 degree C; Prophylactic use of antibiotics; 7. Patients enrolled in other clinical trials in the last three months.

Design outcomes

Primary

MeasureTime frame
Maternal eardrum temperature;

Secondary

MeasureTime frame
Basic vital signs (heart rate, blood pressure, oxygen saturation) and fetal heart rate at each time point;Serum levels of IL - 6, TNF - ? concentration;Epidural sensory blockade level;Labor time;Analgesic time;Apgar score at 1 and 5min;Incidence of maternal nausea, vomiting, itching and respiratory depression;

Countries

China

Contacts

Public ContactLiu Su

Department of Anesthesiology, Affiliated Hospital of Xuzhou Medical University

150040009@qq.com+86 18118309692

Outcome results

None listed

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