Skip to content

Curative effect of Weifuchun on different defrees of atrophic gastritic

Curative effect of Weifuchun on different defrees of atrophic gastritic

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400091096
Enrollment
Unknown
Registered
2024-10-21
Start date
2024-11-01
Completion date
Unknown
Last updated
2024-10-28

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

Conditions

Atrophic Gastritic

Interventions

Observation group:Oral administration of Weifuchun capsules (produced by Hangzhou Huqingyutang Pharmaceutical Co., Ltd., with the approval number Z20040003, specification: 0.35g per capsule) 4 capsul

Sponsors

Xi'an Aerospace General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Age between 18-70 years old; 2. Diagnosed with atrophic gastritis according to the diagnostic criteria of the "Chinese Chronic Gastritis Treatment Guidelines (2022, Shanghai)", with or without intestinal metaplasia and low-grade intraepithelial neoplasia; 3. Hp (Helicobacter pylori) infected patients should first undergo a 14-day Hp eradication treatment.

Exclusion criteria

Exclusion criteria: 1. History of gastric surgery (including endoscopic early cancer, submucosal dissection, and mucosal resection for intraepithelial neoplasia) 2. High-grade intraepithelial neoplasia of the gastric mucosa, gastric cancer, other tumors, severe digestive system diseases, cardiovascular, pulmonary, liver, kidney dysfunction, psychological disorders, pregnant or lactating women; 3. Patients allergic to the ingredients of gastric rejuvenation drugs, currently participating in other clinical trials, having other diseases that may affect this study, or unwilling to undergo follow-up gastroscopy after treatment.

Design outcomes

Primary

MeasureTime frame
Severity of gastric mucosal atrophy and intestinal metaplasia in histopathology before and after treatment;

Secondary

MeasureTime frame
The values of serum pepsinogen (PG I, PG II, PG I/PG II ratio) and gastrin-17 (G-17) before and after treatment.;

Countries

China

Contacts

Public ContactRen Xiaoli

Xi'an Aerospace General Hospital

1169720763@qq.cm+86 134 8832 2017

Outcome results

None listed

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