NCT02047994RecruitingPhase 4
Multicentric Randomized Study of H. Pylori Eradication and Pepsinogen Testing for Prevention of Gastric Cancer Mortality
Source: ClinicalTrials.gov · Last updated 2 May 2025 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
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.
- Status (registry)
- Recruiting
- Phase (registry)
- Phase 4
- Study type
- Interventional
- Enrollment
- 30000 (estimated)
- First submitted
- 27 Jan 2014
- Start date
- Mar 2013
- Primary completion date
- Dec 2033
- Lead sponsor
- International Agency for Research on Cancer
- Diseases
- Gastric and esophageal cancer
- NCT number
- NCT02047994
What you commit to
- Study type: Interventional · Phase 4
- Planned participants: 30000
- From Mar 2013 to the primary completion date, Dec 2033
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- H. pylori eradication therapy within 12 months prior to inclusion (irrespective of the treatment result)
Other illness
- Personal history of gastric cancer (prevalent gastric cancer cases will not be revealed at the time of inclusion, and therefore will be included)
- Gastric resections due to benign disease (ulcer suturing and vagotomy are accepted)
- Presence of alarm symptoms for digestive or any other diseases (detailed in the questionnaire or during the physician evaluation)
- Pathological findings at physical investigation suggestive for a serious organic disease (physician evaluation)
- Serious co-morbid condition with life expectancy less than 5 years (physician evaluation)
- Factors otherwise limiting the participation according to the protocol conditions (problems of mobility, etc.)
- Serious psychological conditions/psychiatric disease limiting the possibilities to understand the requirements for diagnostic and/or medical interventions (physician evaluation)
Other
- Low expectations on the compliance for the diagnostic work-up or treatment (physician evaluation)
- Expected loss for the follow-up (e.g. lack of communication possibilities and data entry in the registries, expected travel abroad, etc.) (physician evaluation)
- Signed consent form is not available
Who the study is looking for
- Men and women aged 40-64 at the time of signing the consent form
- Willingness to get involved in the study irrespective in which of the study arms (after detailed information on the potential benefits and risks that this study may confer)
- The person has signed a consent form (including the acceptance of transporting the samples over the borders, as appropriate)
- To be in good health, as determined by a physical examination and history performed by a study physician at enrolment
Age in the registry: 40 years to 64 years · Sex: All · Accepts healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Institute of Clinical and Preventive Medicine, University of Latvia Coordinator of this site? Confirm its status | Riga | Latvia | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.