Epidural analgesia after cesarean section
Conditions
Interventions
group A:The total amount was 120ml, the concentration of ropivacaine was 0.1%, the sufentanil was 50 µg, the pump speed was 3ml/h
group B:The total amount was 160ml, the concentration of ropivacaine was 0.075%, the sufentanil was 50 µg, the pump speed was 4ml/h
group C:The total amount was 240ml, the concentration of ropivacaine was 0.05%, the sufentanil was 50 µg, the pump speed was 6ml/h
Sponsors
the anesthesia department of Liaocheng dongchangfu district maternal and child health care
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Primipara, singleton, head position, full-term pregnancy, ASA I-II level, patients who understanded and were willingness to participate in this clinical trial.
Exclusion criteria
Exclusion criteria: Twin pregnancy and multiple pregnancy; severe obstetric complications such as pregnancy induced hypertension; congenital heart disease;history of using sedative and hypnotic medication prenatal; abnormal blood coagulation
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Analgesic effect; | — |
Secondary
| Measure | Time frame |
|---|---|
| Preoperative general condition ;Neonatal Apgar score at 1 minutes ;Neonatal Apgar score at 5 minutes;Neonatal Apgar score at 10 minutes;SBP;DBP;Heart rate;Anesthesia condition;Adverse reaction; | — |
Countries
China
Contacts
Public ContactQinzheng Zhao
Liaocheng Dongchangfu District Maternal and Child Health Care
Outcome results
None listed