Missoula, Montana 59812


Purpose:

- Assess the antidepressant/anxiolytic effect of creatine in male and female methamphetamine users - Assess creatine's effect on methamphetamine use - Assess the safety of creatine in male methamphetamine users with depression


Criteria:

Inclusion Criteria: - Current primary diagnosis of methamphetamine dependence or abuse, with methamphetamine preferred drug of abuse - Current diagnosis of major depressive disorder (primary or substance-induced) - Current diagnosis of an anxiety disorder (primary or substance-induced) - Current Hamilton Depression Rating scale score > or = to 16 - Current Hamilton Anxiety Scale score > = to 18 - If taking a psychotropic medication for depressed or anxious mood, regimen must be stable for > = to 4 weeks prior to creatine treatment initiation Exclusion Criteria: - Persons unable to provide adequate informed consent - Persons who are at clinically significant suicidal or homicidal risk - Primary substance-related diagnosis other than methamphetamine dependence or abuse - Positive pregnancy test (females only) - History of renal disease - Clinically significant medical or neurological illness identified by history, physical exam and laboratory testing - History of hypersensitivity reaction to creatine


NCT ID:

NCT02568878


Primary Contact:

Principal Investigator
Tracy Hellem, PhD
Montana State University

Tracy Hellem, PhD
Phone: 406 243 2110
Email: tracy.hellem1@montana.edu


Backup Contact:

N/A


Location Contact:

Missoula, Montana 59812
United States

Tracy Hellem, PhD
Phone: 406-243-2110
Email: tracy.Hellem1@montana.edu

Site Status: Recruiting


Data Source: ClinicalTrials.gov

Date Processed: November 18, 2019

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