FAAH Inhibitor Trial for Adults With Tourette Syndrome



Status:Terminated
Conditions:Neurology
Therapuetic Areas:Neurology
Healthy:No
Age Range:18 - 60
Updated:10/31/2018
Start Date:May 2014
End Date:March 2017

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The purpose of this trial is to examine the safety, tolerability and feasibility in the use
of a FAAH inhibitor for the treatment of adults with Tourette syndrome.


Inclusion Criteria:

- Adult between 18-60 years of age

- Meet DSM IV criteria for the diagnosis of Tourette's syndrome

- Significant current tic symptoms: YGTSS total tic score greater than or equal to 22 at
baseline

- On stable psychiatric medication regimen for a minimum of 4 weeks prior to beginning
the trial.

- Accepted method of birth control

Exclusion Criteria:

- Comorbid bipolar disorder, psychotic disorder, substance use disorder, developmental
disorder or intellectual disability (IQ<70).

- Current use of medications that have significant effects on the cannabinoid or
dopamine systems. Subjects will be specifically excluded for recent use (within last 8
weeks) of antipsychotic medications, dopamine agonists or psychostimulants.

- Recent change (less than 4 weeks) in other medications that have potential effects on
tic severity (such as alpha-2 agonists (guanfacine, clonidine or prazosin), SSRIs,
clomipramine, naltrexone, lithium, anxiolytics, topiramate, baclofen etc.). Medication
change is defined to include dose changes or medication discontinuation.

- Recent change in behavioral treatment for Tourette syndrome or comorbid conditions
(i.e. OCD) within the last 4 weeks or initiation of behavioral therapy for tics within
the last 12 weeks.

- Positive pregnancy test or drug screening test

- History of cannabis dependence

- Significant Medical Comorbidity
We found this trial at
1
site
New Haven, Connecticut 06508
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New Haven, CT
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