Epidural anesthesia for cesarean section
Conditions
Interventions
Group CP:15ml of 3% chloroprocaine
Group LF:15ml of 1.73% lidocaine carbonate combined with 50µg of fentanyl
Sponsors
Xiaoshan Hospital Affiliated to Hangzhou Normal University
Eligibility
Sex/Gender
Female
Age
18 Years to 40 Years
Inclusion criteria
Inclusion criteria: 1. ASA I - II; 2. Aged 18-40 years; 3. 150cm = 37 weeks; 5. Caesarean section is scheduled; 6. Patients signed informed consent.
Exclusion criteria
Exclusion criteria: 1. Allergic to drugs used in this study; 2. Spinal deformity; 3. Twin and/or multiple pregnancies; 4. Coagulation dysfunction; 5. Infection at the puncture site; 6. Complicated with gestational diseases (such as gestational hypertension, gestational diabetes, etc.).
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The time from injection of Initial epidural induction dose to T6 of block level; | — |
Secondary
| Measure | Time frame |
|---|---|
| The time from injection of Initial epidural induction dose to T8 of block level;Incidence of administering additional epidural doses;Incidence of esketamine remediation;The incidence of hypotension;Apagr score of neonates;Bromage scores;Patient satisfaction;The highest level of nociceptive block;The incidence of nausea and vomiting; | — |
Countries
China
Contacts
Public ContactJing Yu
Xiaoshan Hospital Affiliated to Hangzhou Normal University
Outcome results
None listed