A Relevance Study Between the Result of Clinical Drug Intervention and Next-generation Sequencing Technology Focused on Refractory Helicobacter Pylori Infection

NCT02806674 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1845

Last updated 2017-10-31

No results posted yet for this study

Summary

Approximately 50% of people in the world are infected with H. pylori, and its eradication rate fail to exceed 80% and even fails into an unacceptable range.Various risk factors for infection include lower socioeconomic status, younger age, and geographic location.In the present study, investigators aimed to perform a prevalence survey about risk factors for H. pylori infection.To obtain the higher eradication of H. pylori and find out the relevance between the diverse infection and clinical drug focused on refractory H. pylori infection.

Conditions

  • Gastritis

Interventions

DEVICE

The eradication times of the patients

The patients who have failed more than 2 eradication courses with standardized treatment were the refractory infection of H. pylori group,and patients who succeeded at the first standardized treatment were the successful treatment group

DEVICE

The result of 13C-urea breath test after treatment

The intervention focused on the results from the result of 13C-urea breath test after treatment.The two groups were treatment based on the antibiotic susceptibility testing. Eight weeks after treatment,a 13C-urea breath test was performed on patients.The successful treatment group were patients with negative in 13C-urea breath tests in the first treatment. The refractory infection of H. pylori group were treatment failure patients after the second standardized treatment.

Sponsors & Collaborators

  • People Hospital of Luohu,Shenzhen

    collaborator UNKNOWN
  • Shenzhen Second People's Hospital

    collaborator OTHER
  • Longhua Branch of Shenzhen People Hospital

    collaborator UNKNOWN
  • The People Hospital of Baoan Shenzhen

    collaborator OTHER
  • Zhiyuan Medical Inspection Institute

    collaborator OTHER
  • The University of Hong Kong-Shenzhen Hospital

    lead OTHER

Principal Investigators

  • Tao Lyu, Doctor · The University of HongKong-Shenzhen Hospital

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
2016-07-31
Primary Completion
2019-06-30
Completion
2019-12-31

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 NCT02806674 on ClinicalTrials.gov