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Application of Lizhong Fuyuanfang combined with Wenpi San acupoint application in the treatment of chronic atrophic gastritis with weak spleen and stomach

Application of Lizhong Fuyuanfang combined with Wenpi San acupoint application in the treatment of chronic atrophic gastritis with weak spleen and stomach

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2000003599
Enrollment
Unknown
Registered
2020-08-21
Start date
2020-10-01
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 with weak spleen and stomach

Interventions

Sponsors

Shanghai Traditional Chinese Medicine Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. The subjects were Asian patients aged 25 to 75 years of age with unlimited duration of disease and gender; 2. All of them were diagnosed as chronic atrophic gastritis by endoscopy before selection; 3. All of them were diagnosed as chronic atrophic gastritis by pathology before selection; 4. 5% of the patients were diagnosed as chronic atrophic gastritis by pathology. Patients who were diagnosed as HP negative by C13 breath test or gastroscopy, or were treated with HP (confirmed to be HP negative by C13 breath test or gastroscopy one month after the end of the course of treatment of western medicine combined with anti-HP); 5. 5% of the patients were confirmed to be negative by C13 breath test or gastroscopy after the end of the course of treatment of western medicine combined with anti-HP. Syndrome differentiation of traditional Chinese medicine is in accordance with the type of spleen deficiency and phlegm and blood stasis; 6. No other Chinese and Western medicine was used for a month; 7. Those who voluntarily participate in this clinical trial and sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with gastric and duodenal ulcers; 2. Patients with upper gastrointestinal bleeding; 3. Gastric mucosa with high grade epithelial neoplastic or pathological diagnosis of suspected malignant transformation; 4. Patients with severe primary heart, liver, kidney, lung, blood system diseases, renal function Cr > normal reference value upper limit, liver function ALT >= normal reference value more than 1.5 times; 5. A patient who is pregnant or breast-feeding; 6. Those with skin diseases or skin allergies do not cooperate with the operator; 7. Mentally ill; 8. The researchers believe that patients who are not suitable for clinical trials, including patients with poor compliance, who cannot insist on medication for 6 months and who do not undergo gastroscopy after treatment, are not suitable for clinical trials.

Design outcomes

Primary

MeasureTime frame
Clinical recovery;Clinical recovery;

Countries

China

Contacts

Public ContactLiu Yan

Shanghai Traditional Chinese Medicine Hospital?

18019760687@189.cn+86 18116070782

Outcome results

None listed

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