Preliminary Characterization of Commercial Kratom Extract Products

NCT06640569 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 16

Last updated 2025-11-17

No results posted yet for this study

Summary

To understand the acute subjective, physiological, and cognitive effects of commercial kratom extract products among US adults who consume these products regularly, and to understand how these products are metabolized by the human body.

Conditions

  • Kratom Pharmacodynamics
  • Kratom Pharmacokinetics

Sponsors & Collaborators

Principal Investigators

  • Kirsten E Smith, MSW, PhD · Johns Hopkins University

Eligibility

Min Age
21 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-11-11
Primary Completion
2027-11-11
Completion
2028-11-01

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06640569 on ClinicalTrials.gov