Epidural labor analgesia
Conditions
Interventions
contrl group: without labor analgesia during vaginal delivery
experimental group:epidural analgesia during vaginal delivery
Sponsors
Women and Children's Hospital, School of Medicine, Xiamen University
Eligibility
Sex/Gender
Female
Age
20 Years to 35 Years
Inclusion criteria
Inclusion criteria: 1. Pregnant women aged 20-35 with a single full term; 2. Parturient women who give birth through vagina; 3. The subjects who agreed to participate in the study and signed the informed consent.
Exclusion criteria
Exclusion criteria: 1. Patients with severe cardiopulmonary disease; 2. Patients with gestational diabetes or PIH; 3. Patients with abnormal liver and kidney function and coagulation function before delivery; 4. Women with cervical dilatation > 3cm; 5. Parturient women with fetal growth restriction or oligohydramnios possibly related to placental dysfunction; 6. Confirmed infection or fever or basic body temperature before delivery >= thirty-seven point five C; 7. The parturient with infection of epidural puncture site or other contraindications; 8. Patients with severe cognitive or mental disorders; 9. Patients who are allergic to the drugs to be used; 10. Subjects who have taken other experimental drugs or are participating in other clinical studies within one month before the study; 11. Other patients who are not suitable for the study according to the clinician.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Visual Analogue Scale/Score; | — |
Secondary
| Measure | Time frame |
|---|---|
| birth process time;complication; | — |
Countries
China
Contacts
Public ContactFei Shuai
Women and Children's Hospital, School of Medicine, Xiamen University
Outcome results
None listed