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Effectiveness of Transcutaneous Electrical Acupoint Stimulation Combined With Press Needle Therapy for Pain Control After Caesarean Section

Effectiveness of Transcutaneous Electrical Acupoint Stimulation Combined With Press Needle Therapy for Pain Control After Caesarean Section

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400086645
Enrollment
Unknown
Registered
2024-07-08
Start date
2024-07-12
Completion date
Unknown
Last updated
2024-07-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

pain control after caesarean section

Interventions

acupuncture group:transcutaneous electrical acupoint stimulation combined with press needle therapy
sham-acupuncture group:sham acupuncture intervention

Sponsors

the First Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Patients undergoing elective caesarean section under spinal-epidural anesthesia, age between 18 and 45 years, normal singleton pregnancy (37-42 weeks), American Society of Anesthesiologists physical status I or III, provided written informed consent.

Exclusion criteria

Exclusion criteria: 1) congenital coagulopathy; 2) alcohol or drug addiction; 3) pre-eclampsia; 4) recent use of analgesic medications; 5) psychiatric disorders; 6) allergy to intradermal needle; 7) previously experienced deqi; 8) inability to understand verbal and written Mandarin; 9) inability to comprehend or use the numeric rating scale pain scoring system or patient-controlled intravenous analgesia pump.

Design outcomes

Primary

MeasureTime frame
total cumulative morphine consumption at 48 h after caesarean section;

Secondary

MeasureTime frame
postoperative pain scores;Perioperative morphine consumption;PCIA usage;analgesic-related adverse effects;acupuncture-related side effects;patient satisfaction;postoperative complications;postoperative rehabilitation;hospital length of stay;

Countries

China

Contacts

Public ContactKe Wei

the First Affiliated Hospital of Chongqing Medical University

wk202448@hospital-cqmu.com+86 159 0236 0621

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026