Analgesia after cesarean section
Conditions
Interventions
Intervention group:Epidural hydromorphone
Sponsors
Nanjing Maternity and Child Health Care Hospital
Eligibility
Sex/Gender
Female
Age
20 Years to 45 Years
Inclusion criteria
Inclusion criteria: A, elective cesarean delivery, singleton, primigravida; B, ASA class I -II; C, gestational week =37 weeks, age 20-45 years; D, no communication disorder and good compliance; E, no contraindication to intralesional anesthesia.
Exclusion criteria
Exclusion criteria: A, have participated in clinical trials of other drugs within the last 3 months. B, have taken or are recently taking opioids or non-steroidal anti-inflammatory drugs 48 h prior to surgery. C, have had postoperative pruritus of the skin. D, have serious medical comorbidities, including pre-eclampsia, gestational diabetes mellitus, gestational heart disease, asthma, etc. E. Preoperative abnormal liver and kidney function. F, patients with intraoperative changes in anesthesia. G, patients who cannot express their will correctly; those who have poor compliance and cannot complete the trial according to the study protocol.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Hydromorphone dose; | — |
Secondary
| Measure | Time frame |
|---|---|
| VAS score;Blood pressure;Heart rate;Satisfaction with postoperative analgesia; | — |
Countries
China
Contacts
Public ContactHongmei Yuan
Women's Hospital of Nanjing Medical University, Nanjing Maternity and Child Health Care Hospital
Outcome results
None listed