Actively Recruiting

Phase 3
Age: 18Years - 59Years
All Genders
NCT02568878

Creatine for Depressed Male and Female Methamphetamine Users

Led by Montana State University · Updated on 2015-12-11

29

Participants Needed

1

Research Sites

78 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

* 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

CONDITIONS

Official Title

Creatine for Depressed Male and Female Methamphetamine Users

Who Can Participate

Age: 18Years - 59Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Current primary diagnosis of methamphetamine dependence or abuse, with methamphetamine as the preferred drug of abuse
  • Current diagnosis of major depressive disorder, either primary or substance-induced
  • Current diagnosis of an anxiety disorder, either primary or substance-induced
  • Hamilton Depression Rating Scale score of 16 or higher
  • Hamilton Anxiety Scale score of 18 or higher
  • If taking psychotropic medication for depression or anxiety, the regimen must be stable for at least 4 weeks before starting creatine
  • Age between 18 and 59 years
Not Eligible

You will not qualify if you...

  • Unable to provide adequate informed consent
  • At clinically significant risk of suicide or homicide
  • Primary substance-related diagnosis other than methamphetamine dependence or abuse
  • Positive pregnancy test (for females only)
  • History of kidney disease
  • Clinically significant medical or neurological illness identified by history, exam, or lab tests
  • History of allergic reaction to creatine

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Montana State University College of Nursing (Missoula campus)

Missoula, Montana, United States, 59812

Actively Recruiting

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Research Team

T

Tracy Hellem, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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