Skip to main content
OpenTrials
Completed

NCT Number: NCT03843502

A Phased Clinical Trial of Dietary Supplemental Kava: Kava Pharmacokinetics

Kava is a dietary supplement on the US market and is experiencing a resurgence of its use. Its pharmacokinetic information, however, is lacking which is important for its future effective usage as a dietary supplement or potentially as a botanical therapeutics. This phased trial, based on the recommendation from NIH, is to collect pharmacokinetic data of kava in healthy subjects.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–50 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

UF CTSI Clinical Research Center

Gainesville, Florida, 32610, United States

About this study

Kava is used in the South Pacific Islands for relaxation and socialization. It is available in the US as a dietary supplement, and was used in Europe in the 1990s to treat mild to moderate anxiety. Some clinical trials suggested kava's efficacy in treating generalized anxiety disorder (GAD), although a recent meta-analysis was inconclusive. While the mechanisms behind kava's anxiolytic activity are not well-established, its clinical use shows no signs of addiction or withdrawal. Kava thus is a promising and potentially novel anxiolytic with a unique mechanism of action. Although kava has been extensively consumed by humans for centuries, its pharmacokinetics have never been characterized in humans. Such knowledge is essential for its future studies of its anxiolytic potential and dose optimization. This study will characterize kava pharmacokinetics, which will set a solid foundation for its future clinical development. To establish kava pharmacokinetics, each participant will take three 75 mg kava capsules in a single dose and the absorption, distribution, metabolism and excretion of kava will be assessed, corresponding to the pharmacokinetic curve. Serum liver biochemistries will then be monitored for up to three months to test liver function response to kava.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Provide informed consent
  • Females of potential childbearing status must use adequate contraceptive precautions

Exclusion criteria

  • Currently taking any medication or supplement other than vitamins
  • Inability to refrain from acetaminophen, alcohol, or other potentially hepatotoxic substances during the study
  • Have a history of liver disease or currently have liver disease.
  • Elevation in serum ALT, AST, ALP or total bilirubin that reaches clinical significance (as determined by the PI) at screening.
  • Have an unstable medical, psychiatric, or neurological condition determined by history taken during the screening visit and a physical examination at the baseline visit.
  • Have a positive urine drug screen for substances of abuse.
  • Currently using tobacco or nicotine containing products of any form

Treatment and study plan

Kava Dietary Supplement

Drug

Participants will be given three 75mg kava capsules.

Other names: Kava metabolites

Primary outcomes

  1. Time to Maximum Concentration of Kava in the Blood

    Time frame: pre-dose to 12 hours post-dose

    Number of hours that it takes for kava metabolites to reach the maximum concentration in the blood based on multiple blood draws over a 12 hour period

Sponsors and collaborators

Lead sponsor

University of Florida

Other

Collaborators

  • National Center for Complementary and Integrative Health (NCCIH)
  • Thorne HealthTech, Inc

Registry information

Acronym: KavaPK

Important dates

Study start
2020
Primary completion
2021
Study completion
2021
First posted
Feb 18, 2019
Registry last updated
Jun 12, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.