About this trial
There are still some unsolved questions regarding population-based screening program for H. pylori infection to prevent gastric cancer, such as how to perform the optimal screening strategies. A prospective, randomized trial will be conducted to compare the acceptability, compliance (/adherence), and accuracy of diagnostic tests in a population-based H. pylori screening and gastric cancer prevention program.
Initially, we planned to recruit 10,000 adults aged ≥20 years who had not previously undergone H. pylori screening or treatment. Eligible participants were to be randomly allocated in a 1:1:1:1 ratio to one of four groups, each receiving a different combination of diagnostic tests. However, a preliminary analysis led to a recalculation of the required sample size. Following the approval of an Institutional Review Board (IRB) amendment, enrollment was discontinued for Group B (HpSA method) and Group D (Two-stage screening method). The final number of participants enrolled in Group B and Group D was 852 and 851, respectively. Groups A (UBT method) and Group C (standard method) will continue to enroll participants through an additional 1:1 randomization until each group reaches a total of 1,350 participants.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Adults aged 20 years or older
Never screened and treated for H. pylori infection
Disqualifiers
Ever undergone gastrectomy
Patients with gastric cancer
Have been screened or tested for H. pylori infection
Ever received H. pylori eradication therapy
Trial design
Parallel
Treatments tested in this trial
UBT
Diagnostic testH. pylori diagnostic test: C13 urea breath test
HPSA
Diagnostic testH. pylori diagnostic test: H. pylori stool antigen test
UBT and HPSA
Diagnostic testH. pylori diagnostic tests: H. pylori serology test, C13 urea breath test
Serology (two stage)
Diagnostic testH. pylori diagnostic test: If H. pylori serology is positive, confirmation UBT will be done.
Treatment groups
Trial outcomes
Primary outcomes
Detection rates of H. pylori infection
The positivity rate of H. pylori infection between different study arms, respectively in ITT and PP analysis.
Secondary outcomes
The compliance(/adherence) of screening tests for H. pylori infection in the two randomized groups
Completion rates of the study (from enrollment to the diagnosis of H. pylori; from enrollment to the treatment of H. pylori infection.
Sponsors and contacts
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