Overview

Treatment With Cannabis Oil Containing CBD Only or 20:1 CBD:THC vs. Placebo of Persons With ADHD

Status:
Not yet recruiting
Trial end date:
2023-12-01
Target enrollment:
0
Participant gender:
All
Summary
ADHD is the most frequent neuro-developmental disorder in childhood and often continues into adolescence and adulthood. Indicated drug treatments for ADHD fall into 2 categories: stimulants (such as methylphenidate and amphetamines) and non-stimulants (such as atomoxetine, guanfacine and clonidine) but some persons cannot tolerate their secondary effects or find them non-effective. In the last decade, medical cannabis products have been researched as possible treatment for neurological and mental diseases such as: Post trauma disorder (PTD), autism (ASD), epilepsy, fibromyalgia (FM) and more. Data on the effects of cannabidiol rich cannabis extract use for ADHD seems promising but is still limited. The aim of this study is to investigate if oral cannabinoids given to adults with ADHD affect the symptoms of the disorder. The main objectives of the study are: 1) to characterize the effects of treatment with cannabis oil on symptoms of ADHD; 2) to compare safety and efficacy of cannabis oil products with different CBD,Cannabidivarin (CBDV), cannabigerol (CBG) and THC ratio; 3) and to measure endocannabinoids, THC and CBD and metabolites levels in the blood of the participants. In this study, participants diagnosed with ADHD will be treated with canabidiol-rich cannabis oil and will follow up weekly during approx.1 month (the study period). Blood tests will be performed before and after treatment. Blood tests include blood count, blood chemistry, hormones profile, phyto- and endo- cannabinoids and their metabolites. Test of Variables of Attention test (TOVA) will be administrated before and after treatment
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Elkana Kohn
Criteria
Inclusion Criteria:

- Participants aged at least 18 y/o diagnosed with ADHD by Diagnostic and Statistical
Manual of Mental Disorders (DSM)

- Participants with a lower than 0 TOVA score or with a higher than 0 score whom as per
investigator opinion suffer from ADHD

- Participants who experienced treatment failure with more than one ADHD conventional
drug

- Participants willing to attend all the visits in the trial.

Exclusion Criteria:

- Participants who were treated with benzodiazepines, antihistamines, etc, in the week
that preceded the trial start.

- Participants suffering from neurologic or psychiatric diseases

- Participants suffering from malignant diseases

- Participants suffering from syndromes or metabolic diseases

- Participants with significant clinical diagnosis that can damage the trial unfolding.
The investigator may include them after the end of the situation which prevented their
previous inclusion.

- Participants breastfeeding, pregnant or not willing to use contraceptives.

- Participants that will not adhere to the protocol as per investigator opinion

- Participants who weight less than 45 kg or more than 120kg or with BMI greater than 30

- Participants participating in another clinical trial which includes drug treatment

- Participants receiving any treatment for ADHD

- Participants using drugs

- Participants using cannabis or products containing cannabinoids, including medical
cannabis.