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A prospective randomized controlled study on the efficacy and safety of wrist-ankle acupuncture in patients with acute moderate to severe abdominal pain

Evaluation of the Efficacy and Safety of Wrist-Ankle Acupuncture in the Treatment of Acute Moderate to Severe Abdominal Pain: A Prospective Randomized Controlled Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000539
Enrollment
Unknown
Registered
2026-03-13
Start date
2026-04-01
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

abdominal pain

Interventions

Real Acupuncture Group:Phloroglucinol Injection and real acupuncture. Acupuncture sites: Select 1-3 areas of the ipsilateral ankle according to the body segment where the patients tender point is loca
Sham acupuncture group:Phloroglucinol Injection and Sham Acupuncture. Acupuncture points: Select the lower 4th area and lower 5th area under non-therapeutic targets.
Conventional treatment group:No acupuncture operation was performed, and only the basic treatment with phloroglucinol injection was given.

Sponsors

Guangdong Provincial Hospital of Chinese Medicine (General Hospital Emergency Department)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Aged 18 to 75 years, regardless of gender; (2) Acute onset of abdominal pain with a reported onset time within one week; (3) Numeric Rating Scale score = 4 points; (4) Physical examination shows abdominal tenderness, rebound tenderness, or signs of peritoneal irritation; (5) Signed the informed consent form and is willing to cooperate with the researchers.

Exclusion criteria

Exclusion criteria: (1) The patient has used analgesics, spasmolytics, or other drugs (including oral and injectable drugs) within 6 hours before the visit; (2) The patient has a history of long-term chronic pain; (3) The skin at the acupuncture site has conditions unsuitable for acupuncture, such as infection, ulcer, scar, tumor, severe bleeding tendency, long-term oral or injectable anticoagulant use, or severe skin edema; (4) The patient has diseases with insensitivity to pain, such as diabetic peripheral neuropathy, or the patient themselves is not very sensitive to pain; (5) The patient has a history of fainting during acupuncture; (6) The patient has obvious psychological disorders or neurological diseases, poor compliance, and cannot receive acupuncture or drug treatment; (7) The patient has received acupuncture within 24 hours; (8) The patient has high cardiovascular risk factors (especially patients after coronary artery bypass grafting, patients with angina pectoris symptoms); (9) The patient has severe liver or kidney function impairment; (10) Female patients who are pregnant or lactating.

Design outcomes

Primary

MeasureTime frame
Pain relief time;Analgesic effect;

Secondary

MeasureTime frame
Anxiety score;Procalcitonin;The recurrence rate of abdominal pain;

Countries

China

Contacts

Public ContactYanfeng Guo

The Second Affiliated Hospital of Guangzhou University of Traditional Chinese Medicine

871136386@qq.com15112908439

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Apr 4, 2026