Pharmacokinetics of Kratom in Ma

Phase 1

• Conditions: Chronic users

• Registration Number: TCTR20140908001
• Lead Sponsor: Faculty of Medicine Ramathibodi Hospital, Mahidol University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Completion: 2013-10-26
• Study Start: 2014-09-08
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Enrolling by invitation
• Sex: All
• Target Recruitment: 10

Inclusion Criteria

The participants who had no underlying diseases, use Kratom regularly more than 6 months, had the positive urine or blood for mitragynine at the 1st hospital visit.

Exclusion Criteria

The participants denied to participate in the study

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pharmacokinetics 1 October 2014 Pharmacokinetic parameter, Clinical trial Phase I

Secondary Outcome Measures

Name	Time	Method
pain 24 hours after intervention numeric pain score,Cost 24 hours after intervention total cost of pain control