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Clinical Study of Manpixiao in the Treatment of Chronic Atrophic Gastritis

Clinical Study of Manpixiao in the Treatment of Chronic Atrophic Gastritis

Status
UNKNOWN
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05493124
Enrollment
180
Registered
2022-08-09
Start date
2021-07-01
Completion date
2023-12-31
Last updated
2022-08-09

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

Conditions

Chronic Atrophic Gastritis

Brief summary

To explore the efficacy and safety of Manpixiao in the treatment of Chronic Atrophic Gastritis.

Interventions

DRUGManpixiao

A traditional Chinese medicine composition

DRUGActive comparator

Other drugs that may have therapeutic effects

Sponsors

Beijing University of Chinese Medicine
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* The age is 18-75 years old, regardless of gender; * Before treatment, the patients were diagnosed as chronic atrophic gastritis (with intestinal metaplasia and dysplasia) by gastroscopy and pathological examination, which met the criteria of the Chinese consensus on chronic gastritis (2017, Shanghai); * Sign the informed consent form.

Exclusion criteria

* Patients with autoimmune gastritis (chronic atrophic gastritis type A), peptic ulcer (a1-h2), reflux esophagitis, gastric polyps, hypertrophic gastritis and other diseases; * Patients with high-grade intraepithelial neoplasia of gastric mucosa, suspected malignant change of gastrointestinal mucosal lesions, and gastrointestinal tumors; * Patients with malignant tumors who have undergone surgery, radiotherapy and chemotherapy in recent 5 years; * Patients with primary diseases such as heart, brain, lung, hematopoietic system and malignant tumors, and subjects with severe diabetes; * Patients with chronic liver and kidney dysfunction before treatment, including ALT \> 1.5 times the upper limit of normal value, blood creatinine (CR) \> 1.5 times the upper limit of normal value, and platelets lower than 1.5 times the lower limit of normal value; * Disabled subjects specified by law (blind, deaf, dumb, intellectual, mental, physical disabilities); * The description of self symptoms is unclear or the investigation is not the author; * Have a history of alcohol abuse; * Allergic constitution or a history of allergy to multiple drugs (more than two or known ingredients in the drug); * Pregnant or lactating women; * According to the judgment of the researcher, other reasons should not be selected.

Design outcomes

Primary

MeasureTime frameDescription
Pathological improvement rate of gastric mucosaThe enrollment inspection shall be completed within one month before enrollment; The examination after treatment should be carried out within 1 month after the completion of treatment.Pathological diagnosis of gastric mucosal tissue samples obtained by gastroscopy

Secondary

MeasureTime frameDescription
Gastric mucosal status under gastroscopeThe enrollment inspection shall be completed within one month before enrollment; The examination after treatment should be carried out within 1 month after the completion of treatment.For the color of gastric mucosa, spots, erosion, bleeding, reduced folds, visible blood vessels and mucosal texture, 0, 1, 2 and 3 points are given according to the levels of none, I, II and III respectively, and 0 and 1 points are given according to the presence or absence of bile reflux. According to the gastroscopy report, score the patients' microscopic results before and after treatment, and take the result change as the secondary index of curative effect. A lower score means a better result.
Score of main symptoms of stomach systemThey were evaluated on the day of enrollment and the day of the end of the treatment processAdopt the table of main symptoms of stomach system based on doctor's report, the specific contents are: epigastric (epigastric) pain, epigastric (epigastric) distension, epigastric (epigastric) blockage, heartburn, acid reflux, belching, anorexia, reduced appetite. Score 0, 1, 2 and 3 points for the severity of each single symptom (none, mild, moderate and severe). The total score of symptoms is the sum of the individual scores. By comparing the changes of individual symptom scores and total symptom scores between groups, lower scores mean better results.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026