Breastfeeding
Conditions
Interventions
non-labor analgesia group:None
Sponsors
Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Eligibility
Sex/Gender
Female
Age
18 Years to 45 Years
Inclusion criteria
Inclusion criteria: 1. Singleton full-term (37-42 weeks) pregnant women aged 18-45 years; 2. ASA I~II; 3. Willingness to breastfeed postpartum; 4. Voluntary labor analgesia, and no contraindication of neuraxial anesthesia (including abnormal blood coagulation function, infection or injury at puncture site, low blood volume or blood pressure, increased intracranial pressure, spinal pathology or severe spinal deformity, nervous system disease or neuropathy); 5. Sign the informed consent form.
Exclusion criteria
Exclusion criteria: 1. Women suffering from breast development defect or being unable to breastfeed; 2. Women with neuropsychiatric diseases or taking antipsychotic drugs; 3. Apgar 5 min less than 7 after birth; 4. Abnormal labor process; 5. Bleeding volume > 500 mL at 24h postpartum; 6. Low birth weight or macrosomia (neonatal weight 4000g); 7. The newborn has the indication of artificial feeding; 8. The neonates were transferred to neonatal department for treatment Postnatal; 9. Other patients considered by the clinician to be unsuitable for the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Lactation initiation time;Breastfeeding rate; | — |
Countries
China
Contacts
Public ContactJing Wu
Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Outcome results
None listed