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 |
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.
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
Click here to add this to my saved trials