RecruitingPhase 4NCT02047994

Multicentric Randomized Study of H. Pylori Eradication and Pepsinogen Testing for Prevention of Gastric Cancer Mortality


Sponsor

International Agency for Research on Cancer

Enrollment

30,000 participants

Start Date

Mar 1, 2013

Study Type

INTERVENTIONAL

Conditions

Summary

Currently no ideal preventive modalities are available for reducing gastric-cancer caused mortality in organized population-based application. The primary objective of the study is to determine if H.pylori screening followed by eradication of positive subjects and endoscopic follow-up of those with serological evidence of atrophic gastritis reduces mortality from gastric cancer in middle-aged people in high-risk areas. The GISTAR study is a multicenter randomized study of H.pylori eradication and pepsinogen testing for prevention of gastric cancer mortality. Altogether 30.000 individuals aged 40-64 years will be enrolled, providing 90% study power to detect at least 35% reduction in gastric cancer mortality at 15 years of follow-up. Participants will be randomly allocated to one of two groups. In the active investigation/management group those positive for H.pylori will be offered eradication therapy and individuals with decreased pepsinogen I/II ratio will be invited for endoscopy. The control group will receive standard health care. The primary endpoint for this trial will be the mortality difference from gastric cancer between the two groups at 15 years or when enough cases accumulate to demonstrate a statistical difference. The study is expected to provide valuable information on the utility for reduction in gastric cancer mortality of: 1) H.pylori eradication in adults on a population-basis, including subjects who may already have pre-malignant lesions; and 2) pepsinogen testing in screening settings. A pilot study of 3,455 individuals prior to the main trial was conducted from October 2013 to December 2016.


Eligibility

Min Age: 40 YearsMax Age: 64 Years

Plain Language Summary

Simplified for easier understanding

This trial is studying whether a two-step approach — first testing for H. pylori bacteria and then checking stomach health markers — can reduce deaths from stomach cancer in adults in Europe. You may be eligible if: you are a man or woman between 40 and 64 years old; you are in good general health; and you are willing to participate whichever study group you are assigned to. You may NOT be eligible if: you have a personal history of stomach cancer; you have had stomach surgery for ulcers; you received H. pylori treatment in the past 12 months; you have alarming digestive symptoms or serious illness; you cannot commit to follow-up due to travel or other reasons; or you have not signed the consent form. Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGTriple therapy

Participants who are positive with Helicobacter pylori in Group1 will receive triple therapy. * Esomeprazole 40 mg bid for 10 days * Clarithromycin 500 mg bid for 10 days * Amoxicillin 1000 mg bid for 10 days


Locations(1)

Institute of Clinical and Preventive Medicine, University of Latvia

Riga, Latvia

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NCT02047994


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