Postoperative Pain
Conditions
Interventions
Control group:Intravenous patient-controlled analgesia pump
Experimental group:Intravenous patient-controlled analgesia pump+ Buccal Acupuncture Therapy, acupoints were selected, including bilateral Sanjiao, lumbar, and sacral acupoints.
Sponsors
Guangzhou Women and Children's Medical Center Liuzhou Hospital
Eligibility
Sex/Gender
Female
Age
20 Years to 40 Years
Inclusion criteria
Inclusion criteria: (1) Postpartum women aged 20-40 who have undergone cesarean section; (2) Pregnancy weeks are 37-41 weeks, parity = 3, and parity = 4; (3) No history of adverse pregnancy and childbirth, no pregnancy complications; (4) The American Society of Anesthesiologists (ASA) classifies physical condition into grades I-II; (5) Having systematic prenatal care and no underlying diseases; (6) Voluntarily participate in this research project and sign an informed consent form.
Exclusion criteria
Exclusion criteria: (1) Those who do not meet the inclusion criteria; (2) Individuals with contraindications to anesthesia; (3) Patients who experience major bleeding or serious complications during surgery; (4) Individuals with mental disorders and cognitive impairments; (5) Those with poor compliance and inflammation or damage at the acupoint operation site.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Visual Analog Scale (VAS) score;Levels of inflammatory cytokines in peripheral blood and expression levels of serum JAK2/STAT3 pathway proteins; | — |
Secondary
| Measure | Time frame |
|---|---|
| The number of compressions of the intravenous patient-controlled analgesia pump, the time of first anal exhaust, the time of first urination, and the time of getting out of bed activity;Adverse reaction indicators; | — |
Countries
China
Contacts
Public ContactHu Jing
Guangzhou Women and Children's Medical Center Liuzhou Hospital
Outcome results
None listed