Abuse Liability and Human Pharmacology of Mephedrone

Brief Summary

The purposes of this study are 1) to evaluate the abuse liability and human pharmacology of mephedrone after oral administration and 2) to compare the pharmacological effects of mephedrone with those obtained after administration of oral 3,4-methylenedioxymethamphetamine (MDMA, ecstasy).

Intervention / Treatment

  • Drug: Mephedrone
  • Drug: 3,4-methylenedioxymethamphetamine
  • Drug: Placebo

Condition or Disease

  • Amphetamine-Related Disorders

Phase

Study Design

Study type: Interventional
Status: Completed
Study results: No Results Available
Age: 18 Years to 45 Years   (Adult)
Enrollment: 12 ()
Funded by: Other

Masking

Clinical Trial Dates

Start date: Sep 01, 2014
Primary Completion: Dec 01, 2014
Completion Date: Dec 01, 2014
Study First Posted: Sep 05, 2014
Results First Posted: Aug 30, 2020
Last Updated: Dec 04, 2014

Sponsors / Collaborators

Lead Sponsor: N/A
Responsible Party: N/A

Location

Mephedrone is a new psychoactive substance (NPS). At present, there are no randomized controlled trials evaluating the effects of mephedrone in humans. The current body of knowledge regarding the acute effects of mephedrone is based on anecdotal, self-reported effects (e.g. internet forums), case reports, and emergency room series and fatalities.

The aims of this study are 1) to evaluate the abuse liability and human pharmacology of mephedrone after oral administration and 2) to compare the pharmacological effects of mephedrone with those obtained after administration of oral 3,4-methylenedioxymethamphetamine (MDMA, ecstasy).

Eligibility Criteria

Sex: Male
Minimum Age: 18
Maximum Age: 45

More Details

NCT Number: NCT02232789
Other IDs: IMIMFTCL/MEF/1
Study URL: https://ClinicalTrials.gov/show/NCT02232789
Last updated: Jun 16, 2022