Efficacy of a Therapeutic Combination of Dronabinol and PEA for Tourette Syndrome
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|ClinicalTrials.gov Identifier: NCT03066193|
Recruitment Status : Unknown
Verified February 2017 by Yale University.
Recruitment status was: Recruiting
First Posted : February 28, 2017
Last Update Posted : March 3, 2017
|Condition or disease||Intervention/treatment||Phase|
|Tourette Syndrome||Drug: Dronabinol Dietary Supplement: Palmotoyletahnolamide||Phase 3|
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||18 participants|
|Intervention Model:||Single Group Assignment|
|Intervention Model Description:||Participants will receive two active medications and will be followed-up bi-weekly for 12 weeks.|
|Masking:||None (Open Label)|
|Official Title:||Examining the Efficacy of a Therapeutic Combination of Dronabinol (Synthetic Δ9-tetrahydracannabinol) and Palmitoylethanolamide for Tourette Syndrome|
|Actual Study Start Date :||February 1, 2017|
|Estimated Primary Completion Date :||January 2018|
|Estimated Study Completion Date :||January 2019|
All participants will be titrated up on Dronabinol dose during the first week of the trial (2.5mg Dronabinol for 3 days and then 5mg Dronabinol for 4 days increasing to 10mg Dronabinol for the remainder of the trial). Dronabinol will only be increased to 10mg at the week 1 assessment if the subject is tolerating the 5mg dose of Dronabinol and the Dronabinol may be reduced based on patient side-effects. Participants will be receiving PEA concomitantly.
Participants will receive Dronabinol which will be slowly titrated in the first week of the study. They will be followed for a total of 12 weeks.
All participants will receive two 400mg tablets of PEA daily for the same 12 weeks that they receive the Dronabinol.
Dietary Supplement: Palmotoyletahnolamide
Participants will receive the PEA in a standing dose of 400mg. They will be followed for a total of 12 weeks.
- Improvement in Tic Severity [ Time Frame: 12 weeks ]Yale Global Tic Severity Scale (YGTSS) (Total Tic Score)
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03066193
|Contact: Angeli Landeros, MDfirstname.lastname@example.org|
|Contact: Jessica Johnson, BSemail@example.com|
|United States, Connecticut|
|Yale Child Study Center||Recruiting|
|New Haven, Connecticut, United States, 06520|
|Contact: Angeli Landeros, MD 203-737-4809 firstname.lastname@example.org|
|Principal Investigator:||Michael H. Bloch, MD, MS||Yale University|