Combination of Dronabinol and Clonidine for Cannabis Dependence in Patients With Schizophrenia

Stopped early · Phase 2/Phase 3 · Has a placebo group

Conditions studied: Cannabis Dependence, Marijuana Dependence

In brief

Cannabis use disorders are an important public health problem in the United States, but no effective pharmacotherapies are available to treat these disorders. People with schizophrenia are more likely than healthy people to abuse cannabis. Cannabis use may worsen clinical outcomes in this group, making the identification of pharmacotherapy to treat cannabis dependence in those with schizophrenia important. The investigators intend to test the combination of dronabinol, a cannabinoid agonist, and the α2-adrenergic agonist clonidine, for cannabis dependence in subjects with schizophrenia. The combination of dronabinol and clonidine may alleviate cannabis withdrawal symptoms while allowing treatment-seeking outpatients to benefit from medical management (MM) sessions when they are trying to stop using cannabis. The investigators propose to assess the relationship of dronabinol and clonidine, when added to MM, on cannabis use patterns in cannabis-dependent patients with schizophrenia. Hypothesis: The investigators predict that combination pharmacotherapy of dronabinol and clonidine will significantly reduce cannabis use compared to those receiving placebo.

Key facts

Study ID

NCT01598896

Run by

Mclean Hospital

People needed

12

Starts

2012-05-01

Expected to finish

2017-08-01

Last updated by the study team

2018-08-29

Who can join

Age: 18 and older, up to 45. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Age range 18-45 years
• DSM-IV diagnosis of cannabis dependence, based on the Structured Clinical Interview for DSM-IV (SCID)
• DSM-IV diagnosis of schizophrenia or schizoaffective disorder, based on the Structured Clinical Interview for DSM-IV (SCID)
• express a desire to quit cannabis use within the next 30 days
• have used cannabis on ≥20 days within the past 30 days (i.e., an average of ≥5 day per week)
• identify cannabis as their primary drug of abuse; 6) stable on antipsychotic medication for ≥1 month
• for women of childbearing age, a negative pregnancy test at screening with agreement to use adequate contraception to prevent pregnancy and monthly pregnancy tests
• consent for us to communicate with their prescribing clinician if one exists
• furnish the names of 2 locators, who would assist study staff in locating them during the study period
• live close enough to McLean Hospital to attend study visits
• plan to stay in the Boston area for the next 3 months
• are willing and able to sign informed consent.

You may not qualify if…

• Current diagnosis of other drug or alcohol dependence (excluding nicotine)
• significant cardiac disease as indicated by history or suspected by abnormal ECG or history of cardiac symptoms
• Positive and Negative Syndrome Scale (PANSS) subscale for positive symptoms of psychosis item > 3 (moderate) at baseline evaluation
• current medical condition that could prevent regular study attendance
• liver function tests >3 times the upper limit of normal range
• history of seizure disorder or history of head trauma or CNS insult that could predispose the subject to seizures
• taking clozapine
• current suicidal risk
• bradycardia less than or equal to 50 bpm, supine blood pressure of less than or equal to 100/65, a seated blood pressure of less than or equal to 90/60, or orthostatic change of >20 systolic or >10 diastolic on standing, at screening or any pre-dose assessment, or symptoms attributable to low BP (i.e. lightheadedness or dizziness on standing)
• mental retardation or organic mental disorder
• currently in a residential treatment setting in which substance use is monitored and restricted, since the restricted access to drugs could represent an important confounding variable
• pregnant, nursing, or, if a woman of childbearing potential, not using a form of birth control judged by the investigator to be effective
• concomitant treatment with opioid analgesics, sedative hypnotics, or other known CNS depressants
• known hypersensitivity to cannabinoids or sesame oil or clonidine
• disease of the gastrointestinal system, liver, or kidneys that may impede metabolism or excretion of dronabinol
• inability to read or write in English that would hinder their ability to follow study procedures
• history of seizures or a family history of seizures.

Where it is running

• McLean Hospital — Belmont, Massachusetts, United States

Full record on ClinicalTrials.gov

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