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A randomized controlled clinical study of electroacupuncture for improving abdominal bloating in patients after ERCP

A randomized controlled clinical study of electroacupuncture for improving abdominal bloating in patients after ERCP

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026001683
Enrollment
Unknown
Registered
2026-07-06
Start date
2026-07-03
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Choledocholithiasis

Interventions

electroacupuncture group:electroacupuncture
Sham electroacupuncture group:non-acupoint electroacupuncture

Sponsors

Putuo District Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.Age between 18 and 75 years, regardless of gender; 2.Diagnosed with choledocholithiasis and having undergone therapeutic ERCP for the first time; 3.Postoperative baseline VAS score for abdominal distension =3 (on a 0–10 scale); 4.Willing to receive acupuncture treatment and having provided written informed consent. If any of the above is answered "no", the subject cannot be enrolled.

Exclusion criteria

Exclusion criteria: 1.Preexisting conditions causing abdominal distension before surgery, such as chronic functional abdominal distension, irritable bowel syndrome, chronic constipation, or other functional gastrointestinal disorders; 2.Long-term use of medications affecting gastrointestinal motility (e.g., opioid analgesics, anticholinergics, calcium channel blockers) before surgery, and unable to discontinue them after surgery; 3.Any condition that, in the acupuncturist's assessment, makes acupuncture unsuitable for the patient (e.g., skin lesions at the treatment site, presence of a cardiac pacemaker, etc.); 4.Psychiatric disorders, cognitive impairment, or inability to cooperate with VAS scoring. If any of the above is answered "yes", the subject cannot be enrolled.

Design outcomes

Primary

MeasureTime frame
Visual Analogue Scale for Abdominal Distension and Pain;Number of effective gastric peristalsis;

Secondary

MeasureTime frame
Time to first flatus and first defecation;Antral area;

Countries

China

Contacts

Public ContactKai Xia

Putuo District Central Hospital

xk1872040853@163.com18772963329

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Aug 10, 2026