Registry for the Management of Helicobacter Pylori Infection in Shandong Province

NCT07335406 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 10000

Last updated 2026-04-02

No results posted yet for this study

Summary

Helicobacter pylori infection is a common global gastrointestinal infectious disease, affecting approximately 43.1% of the world's population. Eradicating H. pylori is crucial for reducing the risk of developing conditions such as gastritis, peptic ulcer disease, and gastric cancer. Currently, 14-day high-dose dual therapy containing amoxicillin and bismuth-containing quadruple therapy are the guideline-recommended first-line treatment regimens for H. pylori eradication. Treatment options for H. pylori vary considerably, with differing efficacy outcomes largely attributable to increasing bacterial antibiotic resistance. Furthermore, multiple factors influence the efficacy of H. pylori eradication, including smoking, body surface area, CYP2C19 gene polymorphisms, patient compliance, and regional variations.

Therefore, to systematically evaluate the efficacy and safety of different treatment regimens alongside the cost-effectiveness of various therapeutic strategies, and to conduct ongoing critical analysis of clinical practice, this study proposes a long-term investigation of real-world clinical practice through a non-interventional cohort study registry. This will assess the effectiveness, safety, and temporal trends of different H. pylori infection treatment regimens, providing real-time evidence to support clinical practice.

Conditions

  • HELICOBACTER PYLORI INFECTIONS

Interventions

OTHER

Doctors prescribe Helicobacter pylori treatment regimens for patients based on current guidelines and consensus statements, tailored to individual circumstance, not involve any intervention procedure.

Doctors prescribe Helicobacter pylori treatment regimens for patients based on current guidelines and consensus statements, tailored to individual circumstance, not involve any intervention procedure.

Sponsors & Collaborators

  • Yueyue Li

    lead OTHER
  • Qilu Hospital of Shandong University

    collaborator OTHER
  • Feicheng People's Hospital

    collaborator UNKNOWN
  • Binzhou Maternal and Child Health Hospital

    collaborator UNKNOWN
  • Jinxiang County People's Hospital

    collaborator UNKNOWN
  • The People's Hospital of Jimo

    collaborator UNKNOWN
  • Zibo Maternal and Child Health Hospital

    collaborator OTHER
  • Yantai Penglai Traditional Chinese Medicine Hospital

    collaborator UNKNOWN
  • Zaozhuang Municipal Hospital

    collaborator OTHER
  • Linyi Yizhou Hospital

    collaborator UNKNOWN
  • Taierzhuang District People's Hospital

    collaborator OTHER
  • Shandong University of Traditional Chinese Medicine

    collaborator OTHER
  • Yuncheng Traditional Chinese Medicine Hospital

    collaborator OTHER
  • Caoxian County Hospital

    collaborator UNKNOWN
  • Qihe County People's Hospital

    collaborator UNKNOWN
  • University Town Hospital, Afiliated Hospital of Shandong University of Traditional Chinese Medicine

    collaborator UNKNOWN
  • Dezhou Hospital Qilu Hospital of Shandong University

    collaborator OTHER
  • The 2nd People's Hospital of Dongying City

    collaborator UNKNOWN
  • Zhangdian District Hospital of Traditional Chinese Medicine

    collaborator UNKNOWN
  • Yantai Zhifu Hospital

    collaborator UNKNOWN
  • Inner Mongolia Autonomous Region International Mongolian Medicine Hospital

    collaborator UNKNOWN
  • Hohhot Second Hospital

    collaborator UNKNOWN
  • Guanxian People's Hospital

    collaborator UNKNOWN
  • Longkou People's Hospital

    collaborator UNKNOWN
  • Linshu County Hospital of Traditional Chinese Medicine

    collaborator UNKNOWN

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-02-01
Primary Completion
2035-11-01
Completion
2035-11-30

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07335406 on ClinicalTrials.gov