- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02188914
Brain Imaging Studies of the Effect of Inhalant Use Disorder
Neurobiología Del Consumo de Substancias Psicoactivas: PET-CT- Inhalables
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
-
Mexico city, Mexico, 14269
- National Institute of Neurology and Neurosurgery Manuel Velasco Suárez
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Males between 18 to 40 years old.
- Subjects must have a diagnosis of inhalant use disorder who are under a treatment program for addictive disorders or normal control without a history of drug abuse or dependency. Control participants must be matches with the inhalant use disorder participants according to age and years of education.
- Subjects in both the inhalant use disorder and control groups will be volunteers who signed informed consent.
Exclusion Criteria:
- Epilepsy or clinically relevant seizures in the last year
- Cognitive impairment evaluated through Mini-Mental State Examination
- Psychosis
- Manic or hypomanic episode
- Moderate or severe suicide risk
- Panic disorder
- Claustrophobia: Subjects will be questioned about their potential discomfort in being in an enclosed space, such as a PET or MRI scanner.
- History of head trauma with loss of consciousness > 30 min.
- Neurological surgical procedures
- Diabetes
- Positive test for hippuric acid
- Current use of antipsychotic medication
- Current illnesses, painful conditions or other disorders, which in the judgment of the investigators, might invalidate the scientific goals of the study or pose undesirable difficulties or risks for subjects
- In the case for magnetic resonance imaging, Individuals who would be unable to undergo a MRI scan, for example, individuals who have metal clips in their body, metallic prostheses (i.e., replacement body parts, such as a hip joint), a pacemaker, or other pieces of metal in their body (shrapnel, metal filings, etc.).
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Inhalant use disorder group
Subjects must have a diagnosis of inhalant use disorder, according to the DSM-5, who are under a treatment program for addictive disorders.
|
|
|
Normal control group
Normal control without a history of drug abuse or dependency.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Brain metabolic activity
Time Frame: Baseline
|
Determine if the inhalant use disorder participants have different brain metabolic activity than healthy controls
|
Baseline
|
|
Abnormalities in the fractional anisotropy
Time Frame: Baseline
|
Determine if the inhalant use disorder participants show abnormalities in the fractional anisotropy than healthy controls
|
Baseline
|
|
Behavioral performance measures on the executive functions
Time Frame: Baseline
|
Determine if the inhalant use disorder participants show neuropsychological impairments relative to healthy controls in attention and executive functions
|
Baseline
|
|
Severity inhalant use disorder
Time Frame: Baseline
|
Determine if the brain metabolic activity is associated with the severity inhalant use disorder. Determine if the abnormalities in the fractional anisotropy are associated with the severity inhalant use disorder. |
Baseline
|
|
Ratings and scores in the Pittsburgh Sleep Quality Index
Time Frame: Baseline
|
The proportion of participants that have good or bad sleep Quality.
|
Baseline
|
|
Age at which inhalants use began
Time Frame: Baseline
|
Determine if the brain metabolic activity is associated with the age at which inhalants use began. Determine if the abnormalities in the fractional anisotropy are associated with the age at which inhalants use began. |
Baseline
|
|
Duration of regular inhalant use
Time Frame: Baseline
|
Determine if the brain metabolic activity is associated with the duration of regular inhalant use. Determine if the abnormalities in the fractional anisotropy are associated with the duration of regular inhalant use. |
Baseline
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Miguel Ángel Mendoza Meléndez, MD, MPH, Institute for Attention and Prevention of Addictions in Mexico City
- Principal Investigator: Nora Estela Kerik Rotenberg, MD, National Institute of Neurology and Neurosurgery Manuel Velasco Suárez.
Publications and helpful links
General Publications
- Villatoro JA, Cruz SL, Ortiz A, Medina-Mora ME. Volatile substance misuse in Mexico: correlates and trends. Subst Use Misuse. 2011;46 Suppl 1:40-5. doi: 10.3109/10826084.2011.580205.
- Yucel M, Takagi M, Walterfang M, Lubman DI. Toluene misuse and long-term harms: a systematic review of the neuropsychological and neuroimaging literature. Neurosci Biobehav Rev. 2008 Jul;32(5):910-26. doi: 10.1016/j.neubiorev.2008.01.006. Epub 2008 Mar 27.
- Aydin K, Sencer S, Demir T, Ogel K, Tunaci A, Minareci O. Cranial MR findings in chronic toluene abuse by inhalation. AJNR Am J Neuroradiol. 2002 Aug;23(7):1173-9.
- Brouette T, Anton R. Clinical review of inhalants. Am J Addict. 2001 Winter;10(1):79-94. doi: 10.1080/105504901750160529.
- Takagi M, Lubman DI, Walterfang M, Barton S, Reutens D, Wood A, Yucel M. Corpus callosum size and shape alterations in adolescent inhalant users. Addict Biol. 2013 Sep;18(5):851-4. doi: 10.1111/j.1369-1600.2011.00364.x. Epub 2011 Sep 29.
- Yucel M, Zalesky A, Takagi MJ, Bora E, Fornito A, Ditchfield M, Egan GF, Pantelis C, Lubman DI. White-matter abnormalities in adolescents with long-term inhalant and cannabis use: a diffusion magnetic resonance imaging study. J Psychiatry Neurosci. 2010 Nov;35(6):409-12. doi: 10.1503/jpn.090177.
- Volkow ND, Fowler JS, Wang GJ. Positron emission tomography and single-photon emission computed tomography in substance abuse research. Semin Nucl Med. 2003 Apr;33(2):114-28. doi: 10.1053/snuc.2003.127300.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 11/13 protocol
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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