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Clinical Trial Summary

The purpose of this study is to determine if the use of prophylactic bismuth subsalicylate (BSS) has an effect on the acquisition of travelers' diarrhea (TD) or antimicrobial resistance (AMR) genes in fecal samples among international travelers who departed from the United States to South East Asia, South Central Asia, or Africa. Our hypotheses will be tested using a double-blinded, placebo controlled randomized clinical trial with participants from a pre-travel health clinic in the United States.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03535272
Study type Interventional
Source Centers for Disease Control and Prevention
Contact
Status Terminated
Phase Phase 3
Start date May 20, 2018
Completion date December 31, 2023

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