Helicobacter Pylori Infection Clinical Trial
Official title:
10-Day Antimicrobial Susceptibility Testing Guided Triple Therapy Versus 14-Day Empirical Tailored Therapy for the First-line Treatment of Helicobacter Pylori Infection-A Randomized Controlled Trail
The purpose of this study is to assess efficacy of 10-day antimicrobial susceptibility test guided triple therapy for the first-line treatment of Helicobacter pylori infection, then comparing it with 14-day empirical tailored therapy to tell which one has a better performance in both efficacy and safety.
Helicobacter pylori(H.pylori), which infects about 50% of the global population, has been
recognized as a main risk factor of multiple gastric pathologies, especially non-cardiac
gastric cancer. Strongly evidence supports that H.pylori eradication is an effective approach
to reduce the incidence of those pathologies. Antimicrobial susceptibility test can pick out
sensitive drugs to kill Helicobacter pylori, and reduce secondary drug resistance. But, there
is a lack of high quality RCT to compare its efficacy with empirical regimen in the
first-line treatment.
Our study aims to assess the efficacy of 10-day antimicrobial susceptibility test guided
triple therapy for the first-line treatment of Helicobacter pylori infection. Comparing this
regimen with 14-day Empirical Tailored Therapy to tell which one is better in clinic
practice. We also want to find whether the 10-day antimicrobial susceptibility test guided
triple therapy has less intestinal dysbacteriosis with a shorter duration.
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