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Research Progress of Electroacupuncture in Treating Chronic Atrophic Gastritis

Research Progress of Electroacupuncture in Treating Chronic Atrophic Gastritis

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2200006094
Enrollment
Unknown
Registered
2022-06-11
Start date
2022-06-01
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

Chronic Atrophic Gastritis

Interventions

Control group:Western medicine
Experimental group:Electroacupuncture combined with western medicine

Sponsors

Nanjing Hospital of Traditional Chinese Medicine affiliated to Nanjing University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. CAG patients who meet the above western diagnostic criteria; 2. Patients with liver and stomach qi stagnation syndrome according to the above TCM diagnostic criteria; 3. Hp negative confirmed by gastroscopy and pathological examination or Hp negative after eradication treatment; 4. Aged between 18 and 75, with no gender limitation; 5. Patients who did not receive acupuncture treatment or any medicine (Traditional Chinese medicine, Western medicine, patent Chinese medicine, etc.) for 14 consecutive days before inclusion; 6. Informed consent of patients should be obtained through communication, and patients should voluntarily and actively cooperate with diagnosis and treatment and other related research processes.

Exclusion criteria

Exclusion criteria: 1. Unclear syndrome differentiation or too many other syndromes, inconsistent with the TCM diagnostic criteria involved in this study; 2. Patients with intraepithelial neoplasia or gastric cancer indicated by gastroscopy or pathological biopsy, metastasis of cancer cells or other systemic malignancies detected by imaging examination; 3. Those who have had previous stomach surgery; 4. Used traditional Chinese and Western medicine to treat the disease and influence the observation of curative effect within 3 months of the onset of this disease; 5. Patients with primary diseases such as serious damage to heart, brain, liver, kidney and hematopoietic system. People with cognitive, language or mental disabilities; 6. Women who are pregnant or planning to become pregnant and women who are breastfeeding; 7. Allergic constitution and those who are allergic to drugs needed in this study; 8. Within six months or are participating in other clinical trials.

Design outcomes

Primary

MeasureTime frame
Standard table of gastric mucosa grading and scoring under gastroscopy;Histopathological grading standard table;TCM syndrome integral record form;

Secondary

MeasureTime frame
GEDPRO - CG scale;Follow-up investigation of recurrence rate;

Countries

China

Contacts

Public ContactZhang Cairong
njszyyzcr@163.com+86 18951755167

Outcome results

None listed

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