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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
ChiCTR
Registry ID
ChiCTR2100050598
Enrollment
Unknown
Registered
2021-09-01
Start date
2021-08-16
Completion date
Unknown
Last updated
2022-05-02

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

Conditions

chronic atrophic gastritis

Interventions

Weierkang tablet treatment group:None

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. Aged 18 to 75 years, gender is not limited; 2. Patients diagnosed with moderate to severe atrophy and/or intestinal metaplasia by upper gastrointestinal endoscopy and gastric mucosal biopsy (at least 1 in gastric antrum and 1 in gastric corpus) within the past three months, namely OLGA/OLGIM II - Patients with stage IV (moderate or more atrophy/metaplasia in at least one part of the gastric antrum and corpus), including those with low-grade intraepithelial neoplasia, and those with high-grade intraepithelial neoplasia who are reluctant to undergo surgical treatment; 3. No H. pylori infection or successful eradication confirmed by 13C-UBT; 4. Voluntarily accept treatment with Weierkang tablets.

Exclusion criteria

Exclusion criteria: 1. History of gastric surgery (including ESD, EMR) or malignant tumor; 2. Patients with contraindications to the study drug or allergic to the study drug; 3. Pregnant and lactating women; 4. History of drug abuse or alcohol abuse in the past 1 year; 5. People with mental disorders; 6. Those who cannot cooperate with the completion of the treatment plan; 7. Refuse to sign the informed consent; 8. Patients who are participating in other clinical trials; 9. Patients who the researchers believe are not suitable for clinical observational studies for other reasons.

Design outcomes

Primary

MeasureTime frame
Histopathological biopsy of gastric mucosa;gastroscopy;

Secondary

MeasureTime frame
Gastrointestinal symptom Rating Scale;

Countries

China

Contacts

Public ContactShi Yonquan

Xijing Hospital of Air Force Military Medical University

shiyquan@fmmu.edu.cn+86 29 84771515

Outcome results

None listed

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