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Clinical research on tailored eradication therapy of Helicobacter pylori infection based on gastric mucosa samples

Clinical research on tailored eradication therapy of Helicobacter pylori infection based on gastric mucosa samples

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300068618
Enrollment
Unknown
Registered
2023-02-25
Start date
2023-02-25
Completion date
Unknown
Last updated
2023-05-22

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

Conditions

Helicobacter pylori infection

Interventions

Tailored therapy group:Tailored triple therapy
High dose dual therapy group:HDDT

Sponsors

Peking University Third Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Patients undergoing gastroscopy in the Department of Gastroenterology of our hospital; (2) Patients in need of primary eradication therapy of H.pylori infection; (3) Age 18-75 years old; (4) Male or female. In combination with the routine test conditions and the diagnostic criteria of Helicobacter pylori infection in our hospital, the determination method of H.pylori infection was Warthin-Starry staining and RUT double positive in mucosal biopsy.

Exclusion criteria

Exclusion criteria: (1) Patients who have taken PPI or potassium channel acid blockers (P-CAB) within two weeks before enrollment and those who have taken bismuth or antibiotics within four weeks before enrollment;(2) Patients with malignant tumor of digestive tract; (3) Patients who have undergone gastric or esophageal surgery; (4) Patients with severe basic diseases; (5) Patients who have previously eradicated Helicobacter pylori; (6) Patients who are allergic to the drugs used in this study; (7) Pregnant or lactating women; (8) Patients unwilling to participate or unable to cooperate with this stud

Design outcomes

Primary

MeasureTime frame
H.pylori eradicationrate;

Secondary

MeasureTime frame
Incidence of adverse reactions;Patient compliace;

Countries

China

Contacts

Public ContactZhiqiang Song

Peking University Third Hospital

szqinputh@163.com18910192576

Outcome results

None listed

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