Atrophic Gastritis Clinical Trial
Official title:
Efficacy and Safety of Using Granules Dendrobii for the Treatment of Chronic Atrophic Gastritis in Subjects With Deficiency of Qi and Yin: a Randomized, Double-blind, Parallel, Placebo-controlled Study
Chronic atrophic gastritis (CAG) is a common and frequently-occurring disease, characterized by atrophy of gastric mucosal epithelium and glands, thinning of the mucosa, thickening of the submucosal muscle layer, intestinal metaplasia, and atypical hyperplasia. The course of the disease is protracted and often recurrent, which seriously affects the work and physical and mental health of the patient. Moreover, epidemiological studies have shown that the risk of gastric cancer in patients with chronic multifocal atrophic gastritis is significantly higher than that of the general population. Because CAG intestinal metaplasia and dysplasia can easily develop into gastric cancer, the World Health Organization (WHO) listed CAG's gastric mucosal atrophy, intestinal metaplasia and dysplasia as precancerous lesions of gastric cancer in 1978. Therefore, reversing and disappearing the precancerous state of gastric cancer is an effective measure to prevent the occurrence of gastric cancer. The cause of CAG is complicated. Modern medicine believes that CAG is closely related to biological factors, physical and chemical factors, immune factors, and genetic factors. At present, there is no specific treatment, but symptomatic treatment is the main treatment. The disease belongs to the categories of "stomach pain" and "suffocation" in traditional Chinese medicine. In many years of surveys and studies in Mainland China, it is found that Dendrobii granules have a good effect on chronic atrophic gastritis. It is planned to explore the possibility, effectiveness and safety of Dendrobii granules in the treatment of chronic atrophic gastritis through clinical trials. 20 subjects will be randomized into the treatment group and placebo group with 18 weeks of treatment.
Status | Recruiting |
Enrollment | 20 |
Est. completion date | August 2024 |
Est. primary completion date | January 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility | Inclusion Criteria: - Fulfill the diagnosis of chronic atrophic gastritis; - TCM syndrome differentiation is deficiency of both qi and yin; - Aged between 18 and 65 years old, regardless of gender; - Volunteer to participate in this clinical trial and sign an informed consent form. Exclusion Criteria: - Patients with peptic ulcer, acid reflux, etc. who need PPI treatment; - Patients with high-grade intraepithelial neoplasia of gastric mucosa or suspected malignant transformation in pathological diagnosis; - Those who have received anti-HP treatment and related treatments in the past two weeks; - Diabetic patients; - Patients with severe heart, liver, kidney, lung, blood system diseases, abnormal renal function Cr test with clinical significance, and liver function ALT = 1.5 times the upper limit of the normal reference value; - People with allergies or a history of allergies to multiple drugs (two or more or the known ingredients in the drug); - Those planning to become pregnant, pregnant or breast-feeding; - Patients with mental illness; - Those who have participated in other drug clinical trials within the past 3 months; - The investigator believes that it is not suitable to participate in this clinical trial. |
Country | Name | City | State |
---|---|---|---|
Hong Kong | The Chinese University of Hong Kong | Hong Kong |
Lead Sponsor | Collaborator |
---|---|
Chinese University of Hong Kong |
Hong Kong,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change of histopathological grading of gastric mucosal atrophy. | Measure the improvement rate of histopathological grading of gastric mucosal atrophy. | 18 weeks | |
Secondary | Histopathological changes of gastric mucosa | Other histopathological changes of gastric mucosa (intestinal metaplasia, dysplasia, chronic inflammatory reaction, activity, HP infection) grade changes by using the Visual Analogue Scale of New Sydney System. Mild, moderate and severe will be the grading of severity. | 18 weeks | |
Secondary | Grading changes of gastric mucosa | Changes in the grading of the gastric mucosa of gastric antrum (including gastric angle) and gastric body (atrophy, intestinal metaplasia, dysplasia, chronic inflammatory reaction, activity, HP infection) by using the Visual Analogue Scale of New Sydney System. Mild, moderate and severe will be the grading of severity. | 18 weeks | |
Secondary | Grading changes of epigastric bloating | The severity of epigastric bloating will be measured by using the scores 0,2,4,6. Which 0 means no symptom and 6 means most severe.
Three gradings will be recorded: Symptom disappeared, improving or unchanged. Symptom disappeared means the score return to 0. Improving means the score decreases from baseline. Unchanged means score remain the same with baseline. |
18 weeks | |
Secondary | Grading changes of epigastric pain | The severity of epigastric pain will be measured by using the scores 0,2,4,6. Which 0 means no symptom and 6 means most severe.
Three gradings will be recorded: Symptom disappeared, improving or unchanged. Symptom disappeared means the score return to 0. Improving means the score decreases from baseline. Unchanged means score remain the same with baseline. |
18 weeks | |
Secondary | The efficacy of TCM syndromes | Traditional Chinese Medicine syndromes such as epigastric bloating, epigastric pain, belching, loss of appetite will be assessed by the Chinese Medicine Practitioner. 4 gradings 0,1,2,3 will be used, which 3 is the most severe. | 18 weeks | |
Secondary | Inflammation changes under OGD | The severity of inflammation of gastric mucosa will be assessed under endoscopy. Four gradings of the severity which are normal, mild, moderate and severe according to the Visual Analogue Scale of New Sydney System. | 18 weeks | |
Secondary | The H. Pylori eradication rate | The H. Pylori eradication rate (positive at baseline) | 18 weeks |
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