Brain Imaging Studies of the Effect of Inhalant Use Disorder

August 15, 2017 updated by: Miguel Ángel Mendoza Meléndez

Neurobiología Del Consumo de Substancias Psicoactivas: PET-CT- Inhalables

Inhalants substance misuse is an important public health problem whose prevalence is approximately 1% in the general population and 7% among high school students in Mexico. Furthermore Inhalants substance misuse has increased in the recent years (Villatoro et al., 2011). According to the Diagnostic and Statistical Manual of Mental Disorders fifth edition (DSM-5) inhalant use disorder is a problematic pattern of use of a hydrocarbon-based inhalant substance leading to clinically significant impairment or distress. There are studies to suggest that long-term exposure to inhalants is associated with structural brain abnormalities, as well as neuropsychological impairments. However many of these studies have been limited to the gross anatomical report, therefore is necessary the use of complimentary techniques which provide a better understanding of brain. To the date there is no evidence of the use of positron emission tomography, and there are few studies have employed other magnetic resonance imaging methodologies such as diffusion tensor imaging that can be used to know the metabolic activity and white matter tract integrity respectively in inhalant use disorder participants. The purpose of this study is evaluates the effects of the inhalant use disorder in the brain. The investigators will be using positron emission tomography (PET), Magnetic Resonance Imaging (MRI) and diffusion tensor imaging (DTI). As well as, this study will examine the impact of inhalants consumption on executive function performance and the transcriptomic changes associated with inhalants consumption. The investigators hope that the data gathered from this study will lead to the development of more effective treatments

Study Overview

Study Type

Observational

Enrollment (Actual)

70

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Mexico city, Mexico, 14269
        • National Institute of Neurology and Neurosurgery Manuel Velasco Suárez

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 40 years (ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Male

Sampling Method

Non-Probability Sample

Study Population

Participants in inhalant use disorder treatment program or Normal Control Subjects volunteers

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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

This is where you will find people and organizations involved with this study.

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

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 1, 2014

Primary Completion (Actual)

July 30, 2016

Study Completion (Actual)

July 30, 2016

Study Registration Dates

First Submitted

July 9, 2014

First Submitted That Met QC Criteria

July 11, 2014

First Posted (Estimate)

July 14, 2014

Study Record Updates

Last Update Posted (Actual)

August 17, 2017

Last Update Submitted That Met QC Criteria

August 15, 2017

Last Verified

August 1, 2017

More Information

Terms related to this study

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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