Bismuth-containing Quadruple Therapy for Helicobacter Pylori First-line Treatment of Different Tetracycline Doses

NCT05431075 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 406

Last updated 2024-03-27

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 dose and frequency of tetracycline 500mg tid or qid of bismuth 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

Included in quadruple eradication medication.

DRUG

Tetracycline tid

Included in quadruple eradication medication.

DRUG

Tetracycline qid

Included in quadruple eradication medication.

DRUG

Bismuth Potassium Citrate

Included in quadruple eradication medication.

DRUG

Colloidal Bismuth Pectin

Included in quadruple eradication medication.

DRUG

Esomeprazole 20mg

Included in quadruple eradication medication.

Sponsors & Collaborators

  • Peking University Care Luzhong Hospital

    collaborator OTHER
  • Yuncheng Traditional Chinese Medicine Hospital

    collaborator OTHER
  • Taierzhuang District People's Hospital

    collaborator OTHER
  • Zhengzhou Central Hospital

    collaborator OTHER
  • Zibo Central Hospital

    collaborator OTHER_GOV
  • 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
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-07-01
Primary Completion
2024-02-01
Completion
2024-02-01

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 NCT05431075 on ClinicalTrials.gov