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A real-world study on the treatment of chronic atrophic gastritis with intestinal metaplasia using Wen Wei San Ji Gao

A real-world study on the treatment of chronic atrophic gastritis with intestinal metaplasia using Wen Wei San Ji Gao

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400082367
Enrollment
Unknown
Registered
2024-03-27
Start date
2024-04-01
Completion date
Unknown
Last updated
2024-04-01

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

Conditions

Chronic atrophic gastritis with intestinal metaplasia

Interventions

Experimental group:Wen Wei San Ji Gao, oral, three times a day, one tablespoon each time (15-18 milliliters)

Sponsors

Shaanxi Provincial Traditional Chinese Medicine Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Only those who possess all of the following items can be included: (1) Patients diagnosed by Western medicine with chronic atrophic gastritis accompanied by intestinal metaplasia; (2) Traditional Chinese medicine syndrome differentiation belongs to those with spleen and stomach weakness and stomach meridian stasis syndrome; (3) Hp negative individuals or those with Hp infection who have undergone eradication treatment and become negative again after one month; (4) Individuals aged between 18 and 75 years old; (5) Those who voluntarily participate in this clinical study and have signed an informed consent form should comply with ethical principles in the process of signing the informed consent form.

Exclusion criteria

Exclusion criteria: Individuals who meet any of the following criteria are not eligible to participate in this experiment: (1) Patients who have undergone previous stomach surgery or require surgery for gastrointestinal diseases; (2) Pregnant or preparing pregnant women (excluding those who require termination of pregnancy), lactating women; (3) Allergic constitution, such as a history of allergies to two or more drugs or foods; Individuals who are known to be allergic to the ingredients of this medicine; (4) Patients who have participated in clinical studies of other drugs within 3 months; (5) According to the researcher's judgment, other patients who are deemed unsuitable to participate in clinical trials, such as other lesions that reduce the likelihood of enrollment or complicate enrollment, such as frequent changes in the work environment, are prone to loss of follow-up;

Design outcomes

Primary

MeasureTime frame
Changes in total score before and after endoscopic histopathological treatment;Changes in single integral score of gastroscopy histopathology before and after treatment;

Secondary

MeasureTime frame
Pathological efficacy and effectiveness;Single symptom efficacy;Traditional Chinese Medicine Syndrome Therapeutic Effect;Changes in measured values of various indicators of gastrointestinal tumor markers before and after treatment;Changes in measured values of gastrin-17 before and after treatment;Changes in measured values of pepsinogen before and after treatment;

Countries

China

Contacts

Public ContactWen Xinli

Shaanxi Provincial Traditional Chinese Medicine Hospital

wxli696@126.com+86 155 9182 1695

Outcome results

None listed

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