Breastfeeding behaviors
Conditions
Interventions
control group:none labour analgesia
Experimental group:With ropivacaine for labor analgesia
Experimental group:With ropivacaine and sufentanyl for labor analgesia
Sponsors
Department of Anesthesiology, the Obstetrics and Gynecology Hospital of Fudan University
Eligibility
Sex/Gender
Female
Age
18 Years to 45 Years
Inclusion criteria
Inclusion criteria: (1) Term, single births, vaginal delivery of primipara, and intending to postpartum breastfeeding; (2) ASA I - II; (3) Aged 18 to 40 years old; (4) communication fluently, can use PCEA analgesic pump; (5) Signed informed consent.
Exclusion criteria
Exclusion criteria: 1. sufentanyl or other allergic to this study; 2. long-term use of narcotic analgesics, sedatives or non-steroidal anti-inflammatory drugs; 3. previous history of neuromuscular disease; 4. history of endocrine diseases; 5. history of allergic disease; 6. history of previous liver and kidney dysfunction; 7. previous history of mental illness; 8. puerperal infection; 9. anesthesia failure or the need to use other drugs to achieve satisfactory analgesic effect; 10. postpartum hemorrhage; 11. nearly three months to participate in other drug clinical researchers; 12. body mass index> 30 kg/m2; 13. The investigators considered it inappropriate to attend clinical trials.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| breast-feeding success ratio; | — |
Secondary
| Measure | Time frame |
|---|---|
| Perterm Infant Breastfeeding Behavior Scale;Apgar score;Satisfaction score;Edinburgh Depression Scale;Breastfeeging Self efficacy Scale Short Form;Multidimensional Scale of Perceived Scial Support; | — |
Countries
China
Contacts
Public ContactHuang shaoqiang
The Obstetrics and Gynecology Hospital of Fudan University
Outcome results
None listed