Clinical study on electroacupuncture for relieving postoperative pain in patients undergoing abdominal surgery

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2100047799

Enrollment

Unknown

Registered

2021-06-26

Start date

2021-07-12

Completion date

Unknown

Last updated

2022-02-28

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

Conditions

Postoperative pain in patients undergoing abdominal surgery

Interventions

Experimental group1:Electroacupuncture plus drug analgesia

Experimental group2:Pseudo electroacupuncture plus drug analgesia

Control group:Drug analgesia

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged >= 18 years; 2. Complete abdominal surgery; 3. Obtaining informed consent.

Exclusion criteria

Exclusion criteria: 1. Surgical site infection; 2. There were skin lesions, redness, and infection at acupuncture points; 3. Postoperative complications, such as bleeding, perforation, obstruction, abdominal compartment syndrome; 4. Regular use of analgesic drugs within half a year before operation; 5. Cardiovascular diseases such as arrhythmia or pacemaker; 6. Receive acupuncture treatment within 6 weeks before operation; 7. Delirium; 8. Pregnancy.

Design outcomes

Primary

Measure	Time frame
Abdominal pain score;	—

Secondary

Measure	Time frame
Abdominal pain score;Dosage of analgesics;Side effects associated with analgesics;Mechanical ventilation time;Days in Intensive Care Unit;Days in hospital;Mortality;	—

Countries

China

Contacts

Public ContactZhang Xian

Shanghai Jiao Tong University Affiliated Sixth People's Hospital

15902152684@163.com+86 15902152684

Outcome results

None listed

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