Status:
COMPLETED
Citicoline Treatment of Methamphetamine Dependence
Lead Sponsor:
Perry Renshaw
Collaborating Sponsors:
National Institute on Drug Abuse (NIDA)
Conditions:
Methamphetamine Dependence
Eligibility:
All Genders
18-45 years
Phase:
PHASE3
Brief Summary
The purpose of the study is to determine if citicoline (a nutritional supplement) is effective in helping people reduce their dependence on methamphetamine. The investigators will use neuroimaging to ...
Detailed Description
This is a prospective, randomized, double-blind, placebo-controlled study, in which we will systematically evaluate the therapeutic effects of citicoline, which may both increase dopamine and normaliz...
Eligibility Criteria
Inclusion
- Methamphetamine Dependent Subject Eligibility:
- Subjects who use methamphetamine as their preferred drug of abuse.
- Subjects must be between the ages of 18 and 45 years.
- Subjects must have recent methamphetamine use (within 6 months of screening).
- Subjects must have an established residence and phone.
- Subjects must be able to give informed consent.
Exclusion
- Significant current or past medical, neurological, or psychiatric co-morbidity including cardiovascular, renal, and endocrine disorder, as identified by medical history.
- Pregnant subjects - due to the unknown effects of MRI on a fetus. In addition, women of childbearing potential who will not practice a medically accepted method of contraception will be excluded. Female subjects who are of child-bearing potential will have to pass a urine pregnancy test before each visit.
- Subjects who, in the investigator's judgment, pose a current serious homicidal or suicidal risk.
- Subjects who will not likely be able to comply with the study protocol.
- Subjects who have any contraindication to an MR scan.
- Hypersensitivity to any of the study drugs or excipients
- Subjects with current DSM-IV diagnosis of a major mental illness. Major illness will be defined as Major Depression, Manic Depression, Schizophrenia, Dissociative Disorder, other psychotic illnesses, Attention-Deficit Hyperactivity Disorder, Post Traumatic Stress Disorder, Borderline Personality Disorder, Reactive Attachment Disorder, and Panic Disorder.
- Predominant alcohol or other substance dependence as preferred drug of abuse.
- Positive HIV test result.
- An individual having any pending legal or criminal charge or action, or who has pending or a reasonable potential for court involvement, or a person who is incarcerated or is in detention, or who is pending or having completed a competency evaluation or commitment procedure.
- Healthy Control Subject Eligibility:
- Inclusion Criteria:
- Subjects must be between the ages of 18 and 45 years.
- Subjects must be able to give informed consent.
- To have an established residence and phone.
Key Trial Info
Start Date :
January 1 2010
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 1 2012
Estimated Enrollment :
104 Patients enrolled
Trial Details
Trial ID
NCT00950352
Start Date
January 1 2010
End Date
December 1 2012
Last Update
February 11 2015
Active Locations (1)
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1
The Brain Institute of the University of Utah
Salt Lake City, Utah, United States, 84108