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Clinical Study and Molecular Mechanism of Spleen and Stomach Peiyuan Decoction in the Treatment of Chronic Atrophic Gastritis with Intestinal Metaplasia

Clinical Study and Molecular Mechanism of Spleen and Stomach Peiyuan Decoction in the Treatment of Chronic Atrophic Gastritis with Intestinal Metaplasia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025000511
Enrollment
Unknown
Registered
2025-03-11
Start date
2022-06-01
Completion date
Unknown
Last updated
2025-04-07

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

Joint Group:Combined moxibustion on the basis of the treatment group 1 time / d each time 30 min
Treatment Group:Treated with Spleen and Stomach Peiyuan Formula, 2 times/d, 1 h after meal
Control group:Rebapatide tablets combined with folic acid tablets both 1 tablet/dose 3 times/d 1 h before meal.

Sponsors

Department of Spleen and Stomach The Second Affiliated Hospital of Anhui University of Traditional Chinese Medicine China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Those who meet the diagnostic criteria by endoscopy and pathological tissue biopsy; (2) Those who have stable vital signs after conventional treatment and the duration of the disease is less than 3 months; (3) Those with clinical manifestations of the digestive tract such as abdominal distension abdominal pain gastric discomfort belching and acid reflux; (4) Those who voluntarily participate in this clinical trial give informed consent and sign the informed consent form; (5) Aged 18 to 75 years old gender is not limited; (6) Those with complete clinical data.

Exclusion criteria

Exclusion criteria: (1) Patients who have taken proton pump inhibitors (PPIs) and other drugs that may affect the function of the digestive tract within the last 2 weeks; (2) Patients who have taken antibiotics in the last 1 month; (3) Those who have a combination of serious digestive tract haematological neurological malignancies and other primary diseases; (4) Patients with conscious disorders; (5) Those with cognitive dysfunction; (6) Those with severe multi-organ failure; (7) Patients with a history of alcohol consumption within 2 weeks; (8) Patients with Helicobacter pylori infection; (9) Patients with allergy to the drug components in this study; (10) Those with imperfect clinical data; (11) Patients who are also participating in other clinical trials.

Design outcomes

Primary

MeasureTime frame
OLGA staging;clinical symptom score;OLGIM staging;Endoscopic gastric mucosal pathological tissue score;PRO scale;

Secondary

MeasureTime frame
incidence of adverse reactions;;

Countries

China

Contacts

Public ContactXuejun Li

The Second Affiliated Hospital of Anhui University of Traditional Chinese Medicine

15755234412@163.com15755234412

Outcome results

None listed

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