epidural related materna fever
Conditions
Interventions
Group Dexmedetomidine:0.4ug/ml dexmedetomidine and 0.075%ropivacaine for labor analgesia
Group Sufentanil:0.3ug/ml sufentanil and 0.075%ropivacaine for labor analgesia
Sponsors
Shanghai First Maternity and Infant Hospital
Eligibility
Sex/Gender
Female
Age
18 Years to 45 Years
Inclusion criteria
Inclusion criteria: ASA class II, gestational weeks > 37 weeks, 18y 5 (VNRS 0-10, where 0 = no pain and 10 = worst pain imaginable) at the request of epidural analgesia were eligible.
Exclusion criteria
Exclusion criteria: Contraindication to neuraxial anesthesia (e.g., bleeding and coagulation disorders, allergy to local anesthetic drugs); accidental dural puncture; allergy to sufentanil, dexmedetomidine, or ropivacaine; having received opioids or sedatives 4 h prior to labor analgesia and delivery within 4 h after the administration of labor analgesia.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| the incidence of fever; | — |
Secondary
| Measure | Time frame |
|---|---|
| IL-6;ccf-mtDNA; | — |
Countries
China
Contacts
Public Contactzhou shuangqiong
Shanghai First Maternity and Infant Hospital
Outcome results
None listed