Efficacy and Safety of Using Granules Dendrobii for the Treatment of Chronic Atrophic Gastritis
Primary Purpose
Atrophic Gastritis
Status
Recruiting
Phase
Phase 2
Locations
Hong Kong
Study Type
Interventional
Intervention
Granules Dendrobii
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Atrophic Gastritis
Eligibility Criteria
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.
Sites / Locations
- The Chinese University of Hong KongRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Active treatment (Granules Dendrobii)
Placebo
Arm Description
6g each, 3 times per day, total 18 weeks
6g each, 3 times per day, total 18 weeks
Outcomes
Primary Outcome Measures
Change of histopathological grading of gastric mucosal atrophy.
Measure the improvement rate of histopathological grading of gastric mucosal atrophy.
Secondary Outcome Measures
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.
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.
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.
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.
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.
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.
The H. Pylori eradication rate
The H. Pylori eradication rate (positive at baseline)
Full Information
NCT ID
NCT05209633
First Posted
December 1, 2021
Last Updated
November 10, 2022
Sponsor
Chinese University of Hong Kong
1. Study Identification
Unique Protocol Identification Number
NCT05209633
Brief Title
Efficacy and Safety of Using Granules Dendrobii for the Treatment of Chronic Atrophic Gastritis
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
Study Type
Interventional
2. Study Status
Record Verification Date
November 2022
Overall Recruitment Status
Recruiting
Study Start Date
November 1, 2022 (Actual)
Primary Completion Date
January 2024 (Anticipated)
Study Completion Date
August 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Chinese University of Hong Kong
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
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.
Detailed Description
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 study of CAG gastric mucosal atrophy and intestinal metaplasia reversal drugs not only has important academic significance, but also has good social and economic benefits, and has a broad market prospect.
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. The Chinese Medicine practitioners in the past have advocated that the main treatment is to nourish the stomach.
For more than two thousand years, a better understanding of Dendrobii used for "thick intestines and stomach", "calm the stomach", "replenish five internal organs and fatigue", and "light body and prolong life". There are many varieties of Dendrobii, especially Dendrobii officinale is the top grade. Dendrobii candidum is combined with American ginseng to nourish qi and nourish yin, nourish the stomach and promote fluid, nourish but not greasy, clear but not hurt the stomach.
This study used the Granules Dendrobii produced by Zhejiang Tianhuang Medical Plant Pharmaceutical Co., Ltd. (Hong Kong proprietary Chinese medicine registration number: HKC-16115). Granules Dendrobii has completed many pharmacodynamic and toxicological studies. In the many years of market investigation and research in Mainland China, it is found that Granules Dendrobii (Hong Kong Chinese Patent Medicine Registration Number: HKC-16115) has a good effect on chronic atrophic gastritis. Granules Dendrobii is suitable for the long-term conditioning and rehabilitation of spleen and stomach diseases that are weakened by spleen and stomach, or due to deficiency and solidification, resulting in spleen and stomach diseases mixed with deficiency and solid. Granules] with Dendrobium candidum as the main ingredient in the treatment of chronic atrophic gastritis has the traditional theoretical basis of Chinese medicine. Now plan to explore the possibility, effectiveness and safety of Granules Dendrobii in the treatment of chronic atrophic gastritis (qi and yin deficiency) through clinical trials.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Atrophic Gastritis
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
Double-blinded study
Allocation
Randomized
Enrollment
20 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Active treatment (Granules Dendrobii)
Arm Type
Experimental
Arm Description
6g each, 3 times per day, total 18 weeks
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
6g each, 3 times per day, total 18 weeks
Intervention Type
Drug
Intervention Name(s)
Granules Dendrobii
Other Intervention Name(s)
Dendrobii
Intervention Description
6g each, 3 times per day, total 18 weeks
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
placebo
Primary Outcome Measure Information:
Title
Change of histopathological grading of gastric mucosal atrophy.
Description
Measure the improvement rate of histopathological grading of gastric mucosal atrophy.
Time Frame
18 weeks
Secondary Outcome Measure Information:
Title
Histopathological changes of gastric mucosa
Description
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.
Time Frame
18 weeks
Title
Grading changes of gastric mucosa
Description
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.
Time Frame
18 weeks
Title
Grading changes of epigastric bloating
Description
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.
Time Frame
18 weeks
Title
Grading changes of epigastric pain
Description
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.
Time Frame
18 weeks
Title
The efficacy of TCM syndromes
Description
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.
Time Frame
18 weeks
Title
Inflammation changes under OGD
Description
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.
Time Frame
18 weeks
Title
The H. Pylori eradication rate
Description
The H. Pylori eradication rate (positive at baseline)
Time Frame
18 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Cho Wing Lo
Phone
35053476
Email
louislo@cuhk.edu.hk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Zhixiu Lin, Professor
Organizational Affiliation
Hong Kong Institute of Integrative Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Chinese University of Hong Kong
City
Hong Kong
Country
Hong Kong
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Zhixiu Lin, PhD
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Efficacy and Safety of Using Granules Dendrobii for the Treatment of Chronic Atrophic Gastritis
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