Epidural labor analgesia and fever during delivery
Conditions
Interventions
Dexmedetomidine group:The dexmedetomidine group received epidural administration of 0.08% ropivacaine and 0.5ug/ml dexmedetomidine
Sufentanil group (control group):Epidural administration of 0.08% ropivacaine and 0.5ug/ml sufentanil in the sufentanil group
Sponsors
Xinjiang Shihezi People's Hospital (Third Affiliated Hospital of Shihezi University School of Medicine)
Eligibility
Sex/Gender
Female
Age
18 Years to 45 Years
Inclusion criteria
Inclusion criteria: ASA (American Society of Anesthesiologists) level 1-2, aged 18-45 years, with a single pregnancy at term between 37-42 weeks.
Exclusion criteria
Exclusion criteria: Patients with preoperative axillary temperature >37.4 ?, severe cardiovascular disease, bradycardia, contraindications for epidural analgesia, cesarean section or induced labor were not included in this study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Body temperature during delivery after epidural analgesia; | — |
Secondary
| Measure | Time frame |
|---|---|
| Conversion rate of cesarean section after childbirth analgesia; | — |
Countries
China
Contacts
Public Contactwu xiuling
Xinjiang Shihezi People's Hospital (Third Affiliated Hospital of Shihezi University School of Medicine)
Outcome results
None listed