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Study on the Efficacy of Weifuchun Tablets in the Treatment of Chronic Atrophic Gastritis

Study on the Efficacy of Weifuchun Tablets in the Treatment of Chronic Atrophic Gastritis:Single-center, prospective study

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800015200
Enrollment
Unknown
Registered
2018-03-13
Start date
2018-03-19
Completion date
Unknown
Last updated
2018-03-19

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

Conditions

Chronic atrophic gastritis

Interventions

Experimental group:treat with proton pump inhibitor for 1 month,meanwhile folic acid tablets and weifuchun tablets for 6 months
Control group:treat with proton pump inhibitor for 1 month,meanwhile folic acid tablets for 6 months

Sponsors

Wuhan Union Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-80 years old, can tolerate digestive endoscopy; 2. Pathological biopsy confirmed as chronic atrophic gastritis; 3. Suitable for medical treatment; 4. Voluntarily join the experiment and sign a written informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients have history of gastric resection,acute gastrointestinal hemorrhage, advanced gastric cancer, and other gastrointestinal malignant tumors; 2. Suffer from diseases that cannot tolerate gastroscopy, including coagulopathy, renal insufficiency, severe cardiopulmonary disease, and fluorescein sodium hypersensitivity; 3. Pregnancy and lactation women; 4. Patients without legal capacity, or have medical and ethical reasons that influence the conduct of the study; 5. Due to the use of certain banned drugs, it is impossible to evaluate the efficacy.

Design outcomes

Primary

MeasureTime frame
Biopsy pathology results;symptom;Endoscopic diagnosis;

Secondary

MeasureTime frame
Pepsinogen and Gastrin;HP detection;

Countries

China

Contacts

Public ContactLin Rong

Wuhan Union Hospital

selinalin35@hotmail.com+86 15629180035

Outcome results

None listed

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