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Clinical Trial Summary

The objective of this study is to see the amount of systemic absorption of a standard dose of dexamethasone oral rinse for patients with symptomatic oral lichen planus (OLP) or oral lichenoid reactions (OLR) and healthy subjects (those who do not have OLP or OLR aka the control group).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06428630
Study type Interventional
Source Tufts University
Contact Vidya Sankar, DMD, MHS
Phone 617-636-3932
Email vidya.sankar@tufts.edu
Status Not yet recruiting
Phase Early Phase 1
Start date September 1, 2024
Completion date September 1, 2027

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