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
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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