Bismuth-containing Quadruple Therapy for Helicobacter Pylori Eradication

NCT05049902 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 1300

Last updated 2023-07-19

No results posted yet for this study

Summary

The researchers collect treatment-naive H.pylori-positive patients from the outpatient clinic. The subjects were randomized to receive a 10-day or 14-day course of quadruple eradication therapy. 6-8 weeks after treatment, the subjects will re-take the 13C-urea breath test. Calculate the eradication rates, adverse reaction rates, patient compliance and cost-effectiveness index of each group.

Conditions

  • Helicobacter Pylori Infection

Interventions

DRUG

Amoxicillin

Use according to the drug combination options selected by each center.

DRUG

Clarithromycin

Use according to the drug combination options selected by each center.

DRUG

Tetracycline

Use according to the drug combination options selected by each center.

DRUG

Metronidazole

Use according to the drug combination options selected by each center.

DRUG

Bismuth Potassium Citrate

Use according to the drug combination options selected by each center.

DRUG

Colloidal Bismuth Pectin

Use according to the drug combination options selected by each center.

DRUG

Vonoprazan fumarate

Use according to the drug combination options selected by each center.

Sponsors & Collaborators

  • Maternity and Child Care Health Center of Dezhou

    collaborator UNKNOWN
  • Heze Municipal 3rd people's hospital

    collaborator UNKNOWN
  • Peking University Care Luzhong Hospital

    collaborator OTHER
  • The People's Hospital of Jimo.Qingdao

    collaborator UNKNOWN
  • Shandong University

    lead OTHER

Principal Investigators

  • Xiuli Zuo, MD,PhD · Qilu Hospital of Shandong University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2021-09-21
Primary Completion
2023-05-30
Completion
2023-06-30

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 NCT05049902 on ClinicalTrials.gov