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Weierkang pills for the treatment of moderate to severe chronic atrophic gastritis: a multicentre, large data real-world study

Weierkang pills for the treatment of moderate to severe chronic atrophic gastritis: a multicentre, large data real-world study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ITMCTR
Registry ID
ITMCTR2100005255
Enrollment
Unknown
Registered
2021-09-01
Start date
2021-08-16
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

Treatment group:Weierkang Pills (Zhejiang Jiahe Pharmaceutical Co., Ltd., 0.32g/tablet) for treatment. Method of administration: 3 tablets/dose orally before meals, 3 times/day, for 6 months.

Sponsors

Xijing Hospital of Air Force Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Age 18-75 years, regardless of gender. (2) Patients with moderate to severe atrophy and/or intestinalization diagnosed by upper gastrointestinal endoscopy and gastric mucosal pathological tissue biopsy (at least 1 in the gastric sinus and at least 1 in the gastric body) within the last three months, i.e., patients with OLGA/OLGIM stage II-IV (moderate or greater atrophy/atrophy in at least one part of the gastric sinus and body), including those with low-grade intraepithelial neoplasia and those with high-grade intraepithelial neoplasia who do not wish to undergo surgical treatment. (3) Individuals who have been confirmed free of H. pylori infection or successfully eradicated by 13C-UBT. (4) Voluntary treatment with Weierkang pills.

Exclusion criteria

Exclusion criteria: (1) History of previous gastric surgery (including post-ESD, EMR) or with malignancy. (2) Patients with contraindications to the study drug or allergies to the study drug. (3) Pregnant and lactating women. (4) A history of drug abuse or alcohol abuse within the last 1 year. (5) Those with psychiatric disorders. (6) Those who are unable to cooperate in completing the treatment protocol (7) Refusal to sign an informed consent form. (8) Patients who are participating in other clinical trials. (9) Patients who, in the opinion of the investigator, are otherwise unsuitable for clinical observational studies.

Design outcomes

Primary

MeasureTime frame
Histopathological biopsy of gastric mucosa;gastroscopy;

Secondary

MeasureTime frame
Gastrointestinal symptom Rating Scale;

Countries

China

Contacts

Public ContactYonquan Shi

Xijing Hospital of Air Force Military Medical University

shiyquan@fmmu.edu.cn029-84771515

Outcome results

None listed

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