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

Who is this study for? Adults aged 40-64
What treatments are being studied? Triple therapy
Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 4
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
Participation Requirements
Sex: All
Minimum Age: 40
Maximum Age: 64
Healthy Volunteers: t
View:

• 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

Locations
Other Locations
Latvia
Institute of Clinical and Preventive Medicine, University of Latvia
RECRUITING
Riga
Contact Information
Primary
Marcis Leja, MD, PhD
marcis.leja@lu.lv
+37 1 29 49 75 00
Backup
Jin Young Park, PhD
parkjy@iarc.fr
+33 4 72 73 81 63
Time Frame
Start Date: 2013-03
Estimated Completion Date: 2035-12
Participants
Target number of participants: 30000
Treatments
Experimental: Group 1:Triple therapy
Among those assigned to Group 1, participants who are Helicobacter pylori positive will receive Triple therapy and/or upper endoscopy. Participants with serological evidence of atrophic gastritis will undergo upper endoscopy and further endoscopic follow-up. H. pylori positive individuals will be offered Helicobacter pylori eradication as appropriate, independently of the pepsinogen results. From subjects in this group, breath samples will also be collected for volatile markers study. In addition, fecal occult blood test (FOBT) will be offered to this group as a benefit to participate in the study.
No_intervention: Group 2:No intervention
Those who assigned to Group 2 will receive no intervention and will be offered FOBT as a benefit of study participation. Any participants who show positive FOBT will be referred to colonoscopy. This will be the benefit to this group together with initial medical evaluation at the time of inclusion. During the follow-up period this group will be offered to consult a specialist when required due to clinical symptoms.
Sponsors
Collaborators: Vanderbilt University, Karolinska Institutet, Technion, Israel Institute of Technology, Academic Histology Laboratory (Latvia), University of Latvia
Leads: International Agency for Research on Cancer

This content was sourced from clinicaltrials.gov