Post-caesarean section pain
Conditions
Interventions
test group:Self-controlled intravenous analgesic pumps using a pain information management system
control group:Enhancing psychological support for postoperative maternal pain
Sponsors
Guang'an People's Hospital
Eligibility
Sex/Gender
Female
Age
20 Years to 35 Years
Inclusion criteria
Inclusion criteria: singleton; full term (37-42 weeks); first caesarean section; age 20-35 years; weight 50-85KG; ASA class I-II; consent to perform caesarean section under lumbar anaesthesia; signed subject informed consent form
Exclusion criteria
Exclusion criteria: History of allergy to local anaesthetics; contraindications to intralesional puncture (coagulation abnormalities, thrombocytopenia, puncture site infection, trauma, etc.); refusal of intralesional anaesthesia; history of previous pelvic/abdominal surgeries; severe pre-eclampsia and eclampsia; severe cardiorespiratory, hepatic, and renal insufficiency; difficult to co-operate with neuropsychiatric disorders; and history of opioid abuse and allergy.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain scores; | — |
Secondary
| Measure | Time frame |
|---|---|
| Sufentanil dosage;Incidence of complications;Postpartum postoperative analgesia satisfaction; | — |
Countries
China
Contacts
Public ContactQin Sulan
Guang'an People's Hospital
Outcome results
None listed