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Metabolomic study on the treatment of functional dyspepsia with acupuncture at acupoints sensitive to force

Metabolomic study on the treatment of functional dyspepsia with acupuncture at acupoints sensitive to force

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025000357
Enrollment
Unknown
Registered
2025-02-19
Start date
2024-08-22
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

Functional dyspepsia

Interventions

Hypoallergenic group:Acupuncture of five hyposensitive acupoints
High sensitivity group:Acupuncture of five highly sensitive acupoints
Waiting for treatment group:No treatment is done

Sponsors

Jiangxi University of Traditional Chinese Medicine Affiliated Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria: (1) Must meet the diagnostic criteria for functional dyspepsia of Rome IV. (2) Age range: between 18 and 75 years old. (3) The course of the disease is more than 6 months. (4) Have not taken any gastrointestinal prokinetic drugs at least 15 days before the start of the experimental study and have not undergone relevant acupuncture therapy. (5) Not participating in other clinical studies. (6) Voluntarily sign the relevant informed consent form and voluntarily participate in this clinical topic. (Only patients who meet the above inclusion criteria will be included in this study)

Exclusion criteria

Exclusion criteria: Exclusion Criteria: Any of the following conditions must be excluded. (1) Patients with cardiovascular endocrine liver kidney digestive system tumor neuropsychiatric diseases. (2) Women who are pregnant or breastfeeding. (3) Those with severe depression and anxiety symptoms. (4) Those who are severely allergic to needles and metals or have allergies. (5) The patient does not obey the randomized enrollment treatment or has an unstable tendency such as poor compliance. (6) Those who are participating in other research projects that affect the results of the subject or are unwilling to sign the informed consent form.

Design outcomes

Primary

MeasureTime frame
Nepean dyspepsia indexNDI;

Secondary

MeasureTime frame
SAS;SDS;

Countries

China

Contacts

Public ContactLi Fang

The Affiliated Hospital of Jiangxi University of Traditional Chinese Medicine

15620602@qq.com13879193707

Outcome results

None listed

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