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Clinical Trials/NCT02192931
NCT02192931
Completed
Phase 4

A Randomized Double-Blind Controlled Trial of Creatine in Female Methamphetamine Users

Perry Renshaw1 site in 1 country65 target enrollmentSeptember 2014

Overview

Phase
Phase 4
Intervention
Creatine monohydrate
Conditions
Depression
Sponsor
Perry Renshaw
Enrollment
65
Locations
1
Primary Endpoint
Hamilton Depression Rating Scale (HAMD) Scores
Status
Completed
Last Updated
last year

Overview

Brief Summary

Methamphetamine (MA) addiction is a public health concern that causes substantial harm to individual users, and imposes an economic burden in the U.S. totaling up to $48.3 billion annually. This study proposes to address a critical aspect of this problem: the lack of any proven, FDA-approved pharmacological treatments for MA users. The proposal combines an intervention designed to improve energy metabolism in the brain, and a neuroimaging technique capable of measuring the neurochemicals that represent cerebral bioenergetic function. The study will replicate and extend a key neuroimaging finding from the investigators recent MA studies: that MA users have decreased phosphocreatine (PCr) levels in the brain, compared to healthy volunteers. Phosphocreatine is the substrate reservoir for the creatine kinase reaction, which reversibly converts PCr into adenosine triphosphate (ATP), the brain's major energy supply, and creatine. Neuronal energy demands are met through a shift in reaction equilibrium, which is designed to maintain the concentration of ATP constant. Research results from the investigators recent study also showed that female MA users have lower brain PCr levels compared to male users. These findings join the converging lines of evidence that MA use is associated with mitochondrial dysfunction, i.e. deficient energy metabolism, in the brain. Frequently, MA users also experience depression, as well as cognitive deficits. Interestingly, both of these entities are also linked to mitochondrial dysfunction in the brain.

The long-term goal of this research program is to define the alterations in brain chemistry that underlie MA use disorders, and to utilize translational magnetic resonance spectroscopy (MRS) neuroimaging to identify rational brain-based treatment targets. Once a hypothesis-driven intervention is identified, MRS can then be further employed in treatment studies, to verify that "target engagement" is achieved. The specific aims of this proposal are an example of this stepwise scientific process: the nutritional supplement creatine will be tested in a randomized, placebo-controlled study of women with MA use disorders, to investigate creatine's effect on cerebral PCr levels, depressive symptoms, and MA usage.

Registry
clinicaltrials.gov
Start Date
September 2014
End Date
January 31, 2023
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Perry Renshaw
Responsible Party
Sponsor Investigator
Principal Investigator

Perry Renshaw

Professor of Psychiatry

University of Utah

Eligibility Criteria

Inclusion Criteria

  • Female gender, ages 18-55 inclusive
  • Current primary diagnosis of MA dependence or abuse, with MA preferred drug of abuse
  • Current diagnosis of Major Depressive Disorder
  • Current HAMD score \> 15
  • Clinical Global Impressions Severity depression score \> 4
  • If currently taking a psychotropic medication for depressed mood, regimen must be stable for \> 4 weeks before randomization

Exclusion Criteria

  • Persons unable to provide adequate consent
  • Persons who are at clinically significant suicidal or homicidal risk
  • Primary substance-related diagnosis other than MA dependence or abuse
  • Comorbid substance dependence diagnosis, other than nicotine (substance abuse diagnoses are not excluded)
  • Positive pregnancy test
  • Positive test for the antibody to the Human Immunodeficiency Virus (HIV)
  • History of renal disease

Arms & Interventions

Creatine monohydrate

5 grams of daily creatine monohydrate for 8 weeks

Intervention: Creatine monohydrate

Placebo

5 g of placebo for 8 weeks

Intervention: Creatine monohydrate

Outcomes

Primary Outcomes

Hamilton Depression Rating Scale (HAMD) Scores

Time Frame: 8-weeks

Change in Hamilton Depression Rating Scale (HAMD) scores will be evaluated over the course of the 8-week treatment period. The HAMD provides an indication of depression and over time provides a valuable guide to progress. Total score ranges from 0 to 54. 0 means no depression and 24 and above means severe depression.

Secondary Outcomes

  • Beck Anxiety Inventory (BAI) Scores(8-weeks)

Study Sites (1)

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