The impact of epidural labor analgesia on Maternal and Infant Outcomes (Retrospective Study+Prospective Study)
Not Applicable
- Conditions
- labor analgesia
- Registration Number
- ChiCTR2400088744
- Lead Sponsor
- The Third Affiliated Hospital of Zhengzhou University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- Not specified
Inclusion Criteria
Full term pregnancy (gestational age = 37 weeks) with a desire for vaginal delivery, ASA classification: Level I or II Level III, who voluntarily participate in the study and sign an informed consent form
Exclusion Criteria
There are contraindications for spinal anesthesia, a history of alcohol or substance abuse, a history of mental illness, or serious pregnancy complications.
Study & Design
- Study Type
- Observational study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Maternal adverse events;Fetal distress;Neonatal asphyxia;
- Secondary Outcome Measures
Name Time Method Maternal fever;postpartum hemorrhage;Respiratory depression;nausea and vomiting;itch;Neonatal hyperbilirubinemia;Neonatal infection;Transfer of parturient to cesarean section;Postpartum depression;Postpartum infection rate;