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Clinical Trial Summary

In this double blind, crossover study participants will take a placebo for 3 weeks each. Gut permeability will be assessed weekly using food-grade sugar molecules. On the second week, participants will take aspirin, which will make their intestine permeable to the sugars. Participants will be asked to provide urine and stool samples to assess gut permeability and microbial communities. No change in permeability to the small sugar probes is anticipated with the probiotic.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03611400
Study type Interventional
Source University of Florida
Contact
Status Completed
Phase N/A
Start date August 22, 2018
Completion date April 15, 2019

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