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Qilian Xiaopi Fang for the Treatment of Chronic Atrophic Gastritis after Helicobacter pylori Eradication: A multicenter, randomized, double-blind, placebo-controlled study

Qilian Xiaopi Fang for the Treatment of Chronic Atrophic Gastritis after Helicobacter pylori Eradication: A multicenter, randomized, double-blind, placebo-controlled study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400084357
Enrollment
Unknown
Registered
2024-05-15
Start date
2024-05-22
Completion date
Unknown
Last updated
2024-08-12

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

Conditions

Chronic atrophic gastritis

Interventions

Experiment group:Qilian Xiaopi prescription
Control group:placebo

Sponsors

Wangjing Hospital of China Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) Previously HP positive, HP has been successfully eradicated, and the eradication time is more than 1 year; (2) Meet the above criteria for the diagnosis of CAG in Western medicine; (3) Before enrollment, electronic gastroscopy and pathological histology confirmed atrophy (reduction of intrinsic glands) with or without IM, without mild or moderate Dys; (4) Age between 35~70 years old, gender is not limited; (5) Subjects are informed and voluntarily sign the informed consent form; (6) Resident in the local area, able to ensure treatment follow-up, and have a certain reading ability; (7) Those who have not taken anticoagulants such as aspirin and warfarin and those who have no coagulation dysfunction.

Exclusion criteria

Exclusion criteria: (1) Autoimmune gastritis (chronic atrophic gastritis type A); (2) Patients with gastric and duodenal ulcers and upper gastrointestinal bleeding; (3) Patients with high-grade intraepithelial neoplasia of the gastric mucosa or suspected malignant transformation by pathological diagnosis; (4) Patients with serious primary diseases such as heart, brain, liver, kidney, lung and blood system; (5) Suffering from mental illness; (6) Pregnant or lactating women (female subjects must use contraception); (7) Those with allergies or a history of allergies to multiple drugs (more than two or known drugs or ingredients in the study); (8) Other circumstances that the investigator considers inappropriate for inclusion; (9) Patients who are participating in clinical trials of other drugs.

Design outcomes

Primary

MeasureTime frame
Improvement rate of OLGA;

Secondary

MeasureTime frame
Improvement rate of OLGIM ;Improvement rate of gastric mucosal gland atrophy ;TCM syndrome evaluation index;Improvement rate of gastric mucosal intestinal metaplasia ;

Countries

China

Contacts

Public ContactWei Wei

Wangjing Hospital of China Academy of Chinese Medical Sciences

sxxtyy@sina.com+86 84739761

Outcome results

None listed

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