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Methamphetamine Use Disorder clinical trials

View clinical trials related to Methamphetamine Use Disorder.

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NCT ID: NCT04614584 Recruiting - Drug Interaction Clinical Trials

Mirtazapine and Methamphetamine Drug-drug Interaction Study

Start date: July 12, 2021
Phase: Phase 1
Study type: Interventional

This is a drug-drug interaction (DDI) study of mirtazapine for methamphetamine (MA) use disorder (MUD) to ensure the safety of this medication in the presence of a relevant dose of MA for people actively-using MA. Aim 1: To determine if mirtazapine alters the cardiovascular response to IV MA. Aim 2: To determine if the pharmacokinetics of IV MA are altered by mirtazapine administration. Aim 3: To evaluate the above aims in the setting of concomitant administration of methadone. This study involves two simultaneous within-subject drug-drug interaction studies, each comprised of 12 participants. A total of 24 subjects will be enrolled who have methamphetamine use disorder who will be classified into 2 groups: (Group 1: no opioids; Group 2: opioid use disorder on methadone maintenance). Subjects will be randomized to the order of mirtazapine and placebo (i.e. one-half will receive mirtazapine first, then placebo; one-half will receive placebo first, then mirtazapine).

NCT ID: NCT04178993 Completed - Clinical trials for Methamphetamine Use Disorder

Behavioral Effects of Drugs (Inpatient): 40 [Methamphetamine, Methylphenidate, Duloxetine]

Start date: September 1, 2019
Phase: Phase 1
Study type: Interventional

This study will evaluate the behavioral effects of methamphetamine during maintenance on placebo, duloxetine, methylphenidate and duloxetine combined with methylphenidate using sophisticated human laboratory methods.

NCT ID: NCT03106571 Terminated - Clinical trials for Methamphetamine Use Disorder

Study of Pomaglumetad and Methamphetamine

POMA-MA-Ph1
Start date: August 1, 2017
Phase: Phase 1
Study type: Interventional

This is the first study of pomaglumetad in humans using methamphetamine. The goal of the study is to determine if pomaglumetad is safe when administered with methamphetamine. If shown to be safe with methamphetamine in the current study, a phase 2 clinical trial of pomaglumetad would be done to begin to find out if pomaglumetad is effective in treating methamphetamine use disorder.

NCT ID: NCT03078075 Completed - Clinical trials for Methamphetamine Use Disorder

Accelerated Development of Additive Pharmacotherapy Treatment (ADAPT-2) for Methamphetamine Use Disorder

ADAPT-2
Start date: May 5, 2017
Phase: Phase 3
Study type: Interventional

This is a double-blind, placebo-controlled, randomized clinical trial evaluating the efficacy of extended-release naltrexone plus bupropion as a combination pharmacotherapy for methamphetamine use disorder. Participants will be randomly assigned to the active medication combination (AMC) group or matching placebo group and will receive medications over the course of 12 weeks. Follow-ups will occur in weeks 13 and 16.

NCT ID: NCT01982643 Completed - Clinical trials for Methamphetamine Use Disorder

Accelerated Development of Additive Pharmacotherapy Treatment for Methamphetamine Use Disorder

ADAPT
Start date: November 2013
Phase: Phase 1/Phase 2
Study type: Interventional

The aim of this 2-stage, 3-site study is to investigate the effectiveness and safety of a combination of extended-release depot naltrexone plus extended-release bupropion as a potential pharmacotherapy for methamphetamine (MA) use disorder.

NCT ID: NCT00572234 Completed - Clinical trials for Methamphetamine Use Disorder

Bupropion in the Treatment of Methamphetamine Dependence

Start date: August 31, 2007
Phase: N/A
Study type: Interventional

Methamphetamine dependence is a significant drug use disorder in the Midwest. While a number of psychosocial and pharmacological treatments have been studied, no specific treatments for methamphetamine have been identified. This study is a collaborative pre-clinical and clinical partnership examining bupropion in the treatment of methamphetamine dependence.