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P-CABs-based Bismuth Quadruple Therapy for Helicobacter Pylori Eradication (PRO-HP)

Y

Yueyue Li

Status

Enrolling

Conditions

Helicobacter Pylori Infection

Treatments

Other: Doctors prescribe Helicobacter pylori treatment regimens for patients based on current guidelines and consensus statements, tailored to individual circumstances,not involve any intervention procedures

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

Bismuth-containing quadruple therapy was recommended as a first-line treatment for Helicobacter pylori infection. This study aimed to compare real-world outcomes of various potassium-competitive acid blockers (P-CABs) -based bismuth quadruple regimens and identify factors influencing treatment failure. A multicenter cohort study was conducted and study outcomes included eradication rates and incidence of adverse events.

Enrollment

1,730 estimated patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients aged 18-70 years, regardless of gender;
  • willing to receive H. pylori eradication therapy;
  • diagnosed with H. pylori infection through at least one of the following methods: rapid urease test, ¹³C/¹⁴C-urea breath test, or histopathological examination.

Exclusion criteria

  • patients with incomplete medical records, including missing treatment details, absence of post-treatment follow-up test results, or failure to complete essential follow-up assessments;
  • patients who received treatment regimens that did not comply with the quadruple regimens specified in this study.

Trial design

1,730 participants in 2 patient groups

vonoprazan-based quadruple therapies
Treatment:
Other: Doctors prescribe Helicobacter pylori treatment regimens for patients based on current guidelines and consensus statements, tailored to individual circumstances,not involve any intervention procedures
tegoprazan-based quadruple therapies
Treatment:
Other: Doctors prescribe Helicobacter pylori treatment regimens for patients based on current guidelines and consensus statements, tailored to individual circumstances,not involve any intervention procedures

Trial contacts and locations

1

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Central trial contact

Yueyue Li

Data sourced from clinicaltrials.gov

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