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Study on infection and prevention of Helicobacter pylori in high altitude population

Study on infection and prevention of Helicobacter pylori in high altitude population

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200063379
Enrollment
Unknown
Registered
2022-09-05
Start date
2022-09-05
Completion date
Unknown
Last updated
2023-04-17

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

Conditions

Helicobacter pylori infection

Interventions

Togorasen combined medication group:Tigorazan combined with amoxicillin for treatment
Bismuth quadruple group:Tigorazen, bismuth potassium citrate, amoxicillin, clarithromycin tablets treatment

Sponsors

945th Hospital of the PLA Joint Logistic Support Force
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Age: 18-70 years old, male or female; 2. Positive urea breath test; 3. No previous H.pylori eradication treatment; 4. Patients or their legal representatives signed informed consent, understanding and agreeing to comply with the study requirements.

Exclusion criteria

Exclusion criteria: 1. The one had used PPI, potassium competitive acid blockers, antibiotics, H2 receptor antagonists, bismuth, probiotics and other drugs in the four weeks before treatment; 2. Pregnant or lactating women, patients with family planning during the study period; 3. During the treatment, non-steroidal anti-inflammatory drugs, adrenocorticosteroids, anticoagulants, alcohol abuse; 4. Patients allergic to the drugs used in the study; 5. There are other serious diseases affecting the evaluation of this study, such as severe liver disease, heart disease, kidney disease, malignant tumor, mental disease, etc.; 6. Patients with previous gastric and esophageal surgery; 7. Participated in other drug studies within the previous three months; 8. Difficulty in completing follow-up or other factors affecting compliance; 9. Failing to sign the informed consent form.

Design outcomes

Primary

MeasureTime frame
13C-urea breath test;

Countries

China

Contacts

Public ContactRui Wang

945th Hospital of the PLA Joint Logistic Support Force

saviola1720@sina.com+86 13684469807

Outcome results

None listed

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