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Clinical study of different eradication regimens for Helicobacter pylori infection in adults in Yangzhou area

Clinical study of different eradication regimens for Helicobacter pylori infection in adults in Yangzhou area

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000040469
Enrollment
Unknown
Registered
2020-11-29
Start date
2020-12-10
Completion date
Unknown
Last updated
2021-03-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

diseases of upper digestive tract

Interventions

Conventional bismuth quadruple therapy group:Rabeprazole + amoxicillin + clarithromycin + bismuth
High-dose dual therapy group:Rabeprazole + amoxicillin
Based on resistance gene therapy group:Rabeprazole + 2 sensitive antibiotics

Sponsors

Affiliated Hospital of Yangzhou University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) Aged 18-70 years, male or female; (2) He presented with discomfort symptoms such as abdominal pain, abdominal distension, acid reflux, belching, nausea, vomiting, hematemesis, and melena; (3) Positive 14C breath test; (4) No previous H. pylori eradication therapy; (5) Patients who have not used antibiotics, bismuth, H2 receptor antagonists and PPI preparations; (6) Agree to gastroscopy to take gastric mucosal biopsy tissue samples for Helicobacter pylori resistance gene detection; (7) Agree to Helicobacter pylori eradication therapy, and willing to cooperate with the doctor for follow-up investigation of eradication efficacy; (8) Signed informed consent.

Exclusion criteria

Exclusion criteria: (1) Patients with a history of esophageal and gastrointestinal surgery; (2) Patients with bleeding, perforation, pyloric obstruction, and cancer complications; (3) Pregnant or lactating women; (4) Patients who cannot avoid alcohol consumption during the trial; (5) Patients with severe liver, kidney, heart, brain, lung, endocrine system, hematopoietic system diseases or other serious diseases that affect the evaluation of this study; (6) Patients with malignant tumors; (7) Patients can not correctly express their complaints, such as psychosis, severe neurosis; (8) Patients who are allergic to the drugs used in this study; (9) Various factors that are difficult to complete follow-up or affect compliance.

Design outcomes

Primary

MeasureTime frame
eradication of Helicobacter pylori;Incidence of adverse reactions;Improvement of gastrointestinal symptoms;

Countries

China

Contacts

Public ContactYanbing Ding

Affiliated Hospital of Yangzhou University

ydbing@yzu.edu.cn+86 13773582299

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026