Evaluation of Saccharomyces Boulardii Combined With Standard Quadruple Therapy for Eradication of Helicobacter Pylori

NCT03688828 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 360

Last updated 2021-10-26

No results posted yet for this study

Summary

The eradication rate of standard quadruple therapy has become less successful due to low compliance and high resistance to the antibiotics. Therefore, it is necessary to develop new treatment strategies that increase the eradication rate and reduce adverse effects. The aims of this prospective study is to investigate the efficacy of Saccharomyces Boulardii sachets for eradication of Hp, compared with standard quadruple therap.

Conditions

  • Helicobacter Pylori Infection

Interventions

DRUG

Saccharomyces boulardii

500mg bid

DRUG

Esomeprazole

20mg bid

DRUG

Amoxicillin

1.0g bid

DRUG

Clarithromycin

0.5g bid

DRUG

Bismuth potassium citrate

0.22g bid

Sponsors & Collaborators

  • Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

    collaborator OTHER
  • Central Hospital of Xiaogan

    collaborator OTHER
  • Xiaogan First People's Hospital

    collaborator UNKNOWN
  • Hubei Aerospace Hospital

    collaborator UNKNOWN
  • The Third People's Hospital of Hubei Province

    collaborator OTHER
  • Wuhan University

    collaborator OTHER
  • Anlu Puai Hospital

    collaborator UNKNOWN
  • Huazhong University of Science and Technology

    lead OTHER

Principal Investigators

  • Bin Cheng, Doctor · Tongji Hospital

  • Yuchong Zhao, Doctor · Tongji Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2018-11-11
Primary Completion
2020-06-10
Completion
2020-12-31

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 NCT03688828 on ClinicalTrials.gov