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Gene detection and evaluation of high-dose dual therapy for helicobacter pylori

Gene detection and evaluation of high-dose dual therapy for helicobacter pylori

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100054889
Enrollment
Unknown
Registered
2021-12-28
Start date
2022-01-01
Completion date
Unknown
Last updated
2022-12-12

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

Conditions

Helicobacter pylori infection

Interventions

HDDT group:HDDT
Traditional quadruple therapy group:Traditional quadruple therapy

Sponsors

Xiamen Changgung Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. Patients aged 18-45 years in the Department of Gastroenterology, Xiamen Changgung Hospital; 2. Patients with existing Hp infection or failure of previous Hp treatment who had stopped taking the drug for more than 6 months were recruited for this study; 3. Complete gastroscopy before eradicating HP.

Exclusion criteria

Exclusion criteria: 1. Taking drugs that may affect the study results (such as PPI, H2 receptor antagonist, antibiotic, bismuth within 4 weeks prior to enrollment); 2. Patients with gastrointestinal malignancy, and previous gastric and esophageal surgery; 3. Allergic to the drugs in the study; 4. Planning pregnancy, pregnancy, breastfeeding and alcohol abusers; 5. Medical conditions or clinical conditions that may interfere with the treatment evaluation of the study, such as liver disease, cardiovascular disease, lung disease, kidney disease, metabolic disease, psychiatric illness, or malignant tumor; 6. Use of adrenal corticosteroids, non-steroidal anti-inflammatory drugs and anticoagulants; 7. Patients with healing/active duodenal or gastric ulcer, gastric mucosa-associated lymphoid tissue lymphoma, atrophic gastritis, intestinal metaplasia, etc.; 8. Participate in other clinical studies within 3 months prior to participating in this clinical study; or incomplete follow-up or noncompliance with study treatment.

Design outcomes

Primary

MeasureTime frame
Helicobacter pylori breath test;

Countries

China

Contacts

Public ContactLiu Wen

Xiamen Changgung Hospital

279790304@qq.com+86 1598086201

Outcome results

None listed

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