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Clinical Trial Summary

This is a pilot, two-arm, randomized, blinded, placebo-controlled cross-over clinical trial to study the safety and effect of 14 days of kava on anxiety and physiologic stress in survivors of cancer and its treatment. Participants will be randomized to take either kava first or placebo first. Kava 75 mg or placebo will be taken three time daily (TID) for 14 days (Period 1), followed by a washout period of 14-28 days. Thereafter, the participant will take either placebo or kava TID for 14 days (Period 2), whichever he/she did not take in Period 1.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06213298
Study type Interventional
Source Masonic Cancer Center, University of Minnesota
Contact Naomi Fujioka, MD
Phone 612-626-6689
Email fujio002@umn.edu
Status Not yet recruiting
Phase Early Phase 1
Start date June 1, 2024
Completion date August 1, 2025

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