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Weiweiqin granule in the treatment of chronic atrophic gastritis: a muticenter, randomized, controlled trial

Weiweiqin granule in the treatment of chronic atrophic gastritis: a muticenter, randomized, controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-16008027
Enrollment
Unknown
Registered
2016-03-01
Start date
2016-03-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

chronic atrophic gastritis

Interventions

Chinese medicine group:take Weiweiqing Granules
The western medicine group:Taking folic acid tablets

Sponsors

The First Affiliated Hospital of Guangzhou University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: To simultaneously satisfy the following criteria: 1. to meet the chronic atrophic gastritis diagnostic criteria of Western medicine; 2. Aged between 18-65 years old; 3. being able to speaking and reading Chinese to communicate and to fill in the questionnaire; 4. signed the informed consent.

Exclusion criteria

Exclusion criteria: Meet one of the following criteria were excluded: 1. there is explanation above the clinical symptoms of the patients with other diseases; 2. chronic esophagitis, Barrett esophagus and gastroesophageal reflux disease, peptic ulcer, gastric polyp (without resection), digestive tract tumor patients; 3. found that endoscopic gastric mucosa high grade intraepithelial neoplasia, pathological diagnosis, malignant gastrointestinal organic diseases; 4. patients with history of abdominal operation; 5. allergic or allergic to many medicines; 6. confusion, dementia, psychosis, neurosis and various serious unwilling to cooperate; 7. with serious the primary cardiovascular disease, liver disease, kidney disease, blood disease, lung disease, autoimmune diseases, or serious diseases affected the survival, such as cancer or aids; 8. pregnant and lactating women; 9. exist cognitive or other damage (such as vision, etc.) and impact on the participants completed self-report; 10. of the pharmaceutical composition ingredients allergies are; is or 4 weeks in other drug clinical trials of patients; 11. investigators have sufficient reason to believe that the participants according to current medical or psychological state is not suitable for researchers to study.

Design outcomes

Primary

MeasureTime frame
Gastroscope and Histopathological index;

Secondary

MeasureTime frame
Serum pepsinogen I and II;The main symptom score;The outcome scale reported by doctor ;The outcome scale reported by patient;

Countries

China

Contacts

Public ContactLIU Feng-bin

Guangzhou University of Chinese Medicine

liufb163@163.com+86 18902296111

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 22, 2026