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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT02952196
Other study ID # 16.181
Secondary ID
Status Withdrawn
Phase Phase 2
First received
Last updated
Start date November 2016
Est. completion date December 2017

Study information

Verified date January 2019
Source Centre hospitalier de l'Université de Montréal (CHUM)
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Addiction to amphetamine is characterized by alternating phases of intoxication and short abstinence, followed by recurrent drug-craving episodes which result in distress and relapse. Addiction involves a number of neurotransmission systems, including the endocannabinoid system (ECBS). It has been demonstarted that cannabidioids can have physiological, anxiolytic and neuroprotective properties. It has been shown to have multiple therapeutic properties for treating anxiety, schizophrenia and interestingly cannabinoids have been shown to be potentially helpful in treating addiction, due to their effects on various neuronal circuits involved in this disorder. The investigators overall hypothesis is that cannabinoids are an interesting pharmacological contender to decrease amphetamine craving and treat amphetamine addiction.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date December 2017
Est. primary completion date December 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - Current DSM-V criteria for amphetamine use disorder - Ability to give valid, informed consent Exclusion Criteria: - Severe and/or unstable hepatic, neurologic (including diagnosis of seizures), cardiac (including arrhythmias) or renal disease, or any other severe or unstable medical condition that precludes safe participation in the study according to the study physician. - Severe psychiatric condition (history of schizophrenia, schizoaffective disorder or bipolar disorder; current acute psychosis, mania or severe suicidality - Any serious medical condition or psychiatric illness that precludes the subject from signing the informed consent form

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
drug administration
administering drug to patient with amphetamine addiction

Locations

Country Name City State
Canada Centre hospitalier de l'Université de Montréal Montreal Quebec

Sponsors (1)

Lead Sponsor Collaborator
Centre hospitalier de l'Université de Montréal (CHUM)

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary assessing amphetamine craving using questionnaire to assess craving and taking vital signs everyday during the study (that will last 3 days for each participants)
See also
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