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临床试验/NCT02192931
NCT02192931已完成4 期

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

Perry Renshaw1 个研究点 分布在 1 个国家目标入组 65 人开始时间: 2014年9月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
65
试验地点
1
主要终点
Hamilton Depression Rating Scale (HAMD) Scores

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 55 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • 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

排除标准

  • 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

研究组 & 干预措施

Creatine monohydrate

Active Comparator

5 grams of daily creatine monohydrate for 8 weeks

干预措施: Creatine monohydrate (Drug)

Placebo

Placebo Comparator

5 g of placebo for 8 weeks

干预措施: Creatine monohydrate (Drug)

结局指标

主要结局

Hamilton Depression Rating Scale (HAMD) Scores

时间窗: 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.

次要结局

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

研究者

发起方
Perry Renshaw
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Perry Renshaw

Professor of Psychiatry

University of Utah

研究点 (1)

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