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Clinical Trial Summary

The design is a randomized, within-subject, crossover, double-blind, placebo-controlled human alcohol laboratory study with one oral dose of 2g probenecid or placebo administered in two laboratory sessions.


Clinical Trial Description

There will be a total of four study visits. Visit 1 is the screening for eligibility (medical and physical examination). On Visits 2 and 3, participants will undergo an alcohol laboratory session with a one week washout period before administering the alternate therapy. The study will conclude at Visit 4. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04218357
Study type Interventional
Source Brown University
Contact
Status Completed
Phase Phase 1
Start date December 2, 2020
Completion date May 20, 2023

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