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A Study of Teprenone on Symptom Improvement in Patients With Autoimmune Gastritis

A Study of Teprenone on Symptom Improvement in Patients With Autoimmune Gastritis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500101891
Enrollment
Unknown
Registered
2025-04-30
Start date
2025-05-05
Completion date
Unknown
Last updated
2025-05-05

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

Conditions

Autoimmune Gastritis

Interventions

Conventional treatment group:Mecobalamin tablets 0.5mg, tid
Folic acid 5mg, qd
Conventional treatment combined with teprenone treatment group:Mecobalamin tablets 0.5mg, tid
Teprenone capsules 50mg/time, tid, with meal

Sponsors

Peking Union Medical College Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Male or female, aged 18-70 years old; 2. Symptoms such as bloating and anorexia; 3. Positive gastroscopy and pathological results and/or serum antibody markers within 3 months prior to enrollment, and the results meet the diagnostic criteria for AIG proposed by the Japanese Society of Gastrointestinal Endoscopy: (1) Severe atrophy of the mucosa from the gastric body to the fundus by endoscopic examination and/or histopathological examination; (2) Positive gastric autoantibodies—positive anti-parietal cell (APCA) and/or anti-intrinsic factor (IFA) antibodies. Those who included (1) and (2) met at the same time; 4. The patient voluntarily signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Untreated patients with active Helicobacter pylori infection; 2. Pathological examination with intraepithelial neoplasia; 3. Accompanied by other gastric mucosal lesions [such as active ulcer, active bleeding, gastric cancer, etc.]; 4. After gastrectomy; 5. Endoscopic treatment for intraepithelial neoplasia and adenoma in the past three months, such as ESD (endoscopic mucosal dissection) and EMR (endoscopic mucosal resection); 6. Those with obvious mental and behavioral abnormalities and emotional disorders; 7. Severe cardiovascular and cerebrovascular diseases, abnormal liver and kidney function; 8. Other malignant tumors are currently under treatment (chemotherapy, radiotherapy, immunotherapy, etc.); 9. Pregnant or lactating women; 10. Allergy to the study drug; 11. Patient has not signed the informed consent form.

Design outcomes

Primary

MeasureTime frame
Clinical Symptom Score;Compliance;

Secondary

MeasureTime frame
Serum index detection;

Countries

China

Contacts

Public ContactLi Jingnan

Peking Union Medical College Hospital

lijn2008@126.com+86 136 0123 5229

Outcome results

None listed

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