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A single-center prospective non-inferiority randomized controlled study comparing the efficacy of Weimisu and Tepuritron in treating precancerous gastric conditions

A single-center prospective non-inferiority randomized controlled study comparing the efficacy of Weimisu and Tepuritron in treating precancerous gastric conditions.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400091936
Enrollment
Unknown
Registered
2024-11-06
Start date
2024-11-10
Completion date
Unknown
Last updated
2024-11-11

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

Conditions

Atrophic gastritis, intestinal epithelial hyperplasia

Interventions

experimental group:Experimental group: vinblastine
Control group:Control group: teprenone

Sponsors

The Seventh Affiliated Hospital Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Age between 18 and 65 years old (inclusive), gender is not limited; 2.The initial diagnosis of gastroscopy and pathology in our hospital met the diagnostic criteria for precancerous diseases of the stomach; 3.Voluntarily participate in this clinical trial, give informed consent and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Autoimmune gastritis (type A chronic atrophic gastritis); 2.People with combined gastric and duodenal ulcers, upper gastrointestinal bleeding or those who need to take other related medications for stomach disorders; 3.Gastric mucosa with high-grade intraepithelial neoplasia, mucosal pathology diagnosis suspecting malignancy; 4.Those with a combination of serious organic diseases, such as serious primary diseases of the heart, brain, liver, kidneys, lungs and haematological system; 5.Persons with a history of allergy to known drugs or ingredients in the study; 6.History of previous gastric surgery (including post-ESD, EMR) or with malignancy; 7.Comorbid severe psychiatric disorders were unable to cooperate with the study; 8.Women who are pregnant or breastfeeding; 9.Patients who are participating in a clinical trial of another drug or who have stopped their last drug study for less than 1 month; 10.Those who cannot co-operate with follow-up visits and investigations refuse to sign the informed consent form; 11.Other conditions that the researcher considers inappropriate for enrolment.

Design outcomes

Primary

MeasureTime frame
Pathohistological changes in the gastric mucosa;

Secondary

MeasureTime frame
Gastrointestinal symptom level assessment scale score, blood inflammatory factors (C-reactive protein (CRP), interleukin-1ß (IL-1ß), tumor necrosis factor-a (TNF-a)), pepsinogen, gastrin, riboflavin;

Countries

China

Contacts

Public ContactYu Hong

The Seventh Affiliated Hospital Sun Yat-sen University

potteryuhong@163.com+86 18640096687

Outcome results

None listed

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