The Effects of Medical Cannabis in Children With Autistic Spectrum Disorder
Primary Purpose
Autism Spectrum Disorder
Status
Active
Phase
Phase 3
Locations
Israel
Study Type
Interventional
Intervention
Cannabis oil
Sponsored by
About this trial
This is an interventional treatment trial for Autism Spectrum Disorder focused on measuring Autism, Cannabis, co-morbid symptoms, ASD, Cannabidiol
Eligibility Criteria
Inclusion Criteria
- diagnosed with ASD by DSM
- IQ below 70. The investigator can include patients with IQ above 70 if they have significant ASD or comorbid symptoms.
- With significant behavior problems in for at least 6 months before recruitment
Exclusion Criteria:
- Epilepsy with clinical symptoms
- Current or previous treatment with cannabis
- Genetic disorder that can cause ASD symptoms
- Metabolic disorder
- immunologic disorder
- liver cancer
- Participants who, in the researcher's opinion, will not cooperate in the various research procedures
- Women which are pregnant or breastfeeding.
- Psychosis or schizophrenia or past or present schizoaffective disorder, in first-degree relatives
- History of substance abuse or abuse (including cannabis use disorder or alcohol addiction) in first-degree relatives
- Hypersensitivity to coconut oil / palm oil
Sites / Locations
- Assaf Harofeh Medical Center
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Seach CBD:THC 20:1 cannabis oil
Candoc CBD:THC 20:1 cannabis oil
Arm Description
cannabis oil containing CBD:THC ratio of 20:1. plant material is grown by Seach LTD and oil manufactured by Nextar Pharma LTD.
cannabis oil containing CBD:THC ratio of 20:1. plant material is grown by Candoc LTD and oil manufactured by Panaxia LTD.
Outcomes
Primary Outcome Measures
Cannabinoids levels change
To compare CBD, THC their and metabolites blood levels before and after intervention
Changes in attention span
To characterize the effect of medical cannabis treatment on the attention span using Conners teacher questionnaires. Significant change is defined as a change of 10% in questionnaire score between baseline and 6 months.
Changes in cognitive level
To examine the effect of cannabis treatment on cognitive level using part of Wechsler test. Significant change is defined as a change of 10% in questionnaire score between baseline and 6 months.
Comparison of efficacy between two different cannabis oil products
To compare efficacy of medical cannabis products with the same CBD: THC ratio in terms of communication skills using ADOS test. Significant change is defined as a change of 10% in raw questionnaire score between baseline and 6 months.
Changes in adaptive behavior
To examine the effect of cannabis treatment on adaptive behavior as per ADOS test. Significant change is defined as a change of 10% in raw questionnaire score between baseline and 6 months.
Changes in violent behavior
To examine the effect of cannabis treatment on violent behavior as per specific trial-designed questionnaire. Significant change is defined as a change of 10% in questionnaire score between baseline and 6 months.
Secondary Outcome Measures
Side effects
To identify side effects as per parents report in a specific trial-designed questionnaire. Significant change is defined as a change of 10% in new side effects as examined by questionnaire score between baseline and 6 months.
Therapeutic failure
To identify therapeutic failure reasons as per Professional expert opinion. Significant reason is defined as reason that will effect at least 20% of therapeutic failure cases.
Changes in sleep problems
To examine whether high concentration CBD cannabis oil is effective in improving sleep as per Sleep questionnaire. Significant change is defined as a change of 10% in raw questionnaire score between baseline and 6 months.
Changes in eating problems
To examine whether high concentration CBD cannabis oil is effective in improving eating as per eating questionnaire. Significant change is defined as a change of 10% in raw questionnaire score between baseline and 6 months.
Changes in hormonal profile
To compare hormonal profile measured as per by Hospital Lab SOP before and during treatment. measured hormones are: TSH, FT4, 17OH-testosterone, LH, prolactine. Significant change is defined as a clinically significant diversion from lab defined normal ranges, according to age and sex, between baseline and 3 months.
Changes in biochemical parameters
To compare liver enzymes measured as per by Hospital Lab SOP before and during treatment. Measured enzymes are: ALT, AST, GGT, Bilirubin. Significant change is defined as a clinicaly significant diversion (more than twice the Upper Limit of Noraml for each enzyme) from lab defined normal ranges, between baseline and 3 months.
Full Information
NCT ID
NCT05212493
First Posted
December 12, 2021
Last Updated
January 31, 2023
Sponsor
Assaf-Harofeh Medical Center
Collaborators
Seach Sarid Ltd, Canndoc Ltd
1. Study Identification
Unique Protocol Identification Number
NCT05212493
Brief Title
The Effects of Medical Cannabis in Children With Autistic Spectrum Disorder
Official Title
The Effects of Medical Cannabis in Children With Autistic Spectrum Disorder
Study Type
Interventional
2. Study Status
Record Verification Date
January 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
November 14, 2019 (Actual)
Primary Completion Date
December 31, 2021 (Actual)
Study Completion Date
December 31, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assaf-Harofeh Medical Center
Collaborators
Seach Sarid Ltd, Canndoc Ltd
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Children with autism spectrum disorder (ASD) commonly exhibit comorbid symptoms such as aggression, hyperactivity and anxiety. Data on the effects of cannabidiol rich cannabis extract use for ASD is promising but still limited. The aim of this study is to investigate if oral cannabinoids treatment to children and young adults with ASD affect the comorbidities of autism, including sleep and eating problems, anxiety and violence.
The main objectives of the study are: 1) to characterize the effect of treatment with cannabis oil on comorbid symptoms of ASD; 2) to compare safety and efficacy of different cannabis products with identical CBD:THC ratio; 3) to investigate the effect of treatment on cognitive and adaptive behavior; and 4) to measure THC and CBD and metabolites levels in the blood of the patients.
In this study, patients diagnosed with ASD will be treated with cannabidiol-rich cannabis oil (CBD:THC ratio of 20:1). The researchers will collect parental reports on ASD comorbid symptoms before and bi-weekly during 6 months of the study period. Blood tests will be performed before and after three months of treatment. Blood tests include blood count, blood chemistry, hormones profile, phyto- and endo- cannabinoids and metabolites. Cognitive evaluation will be done before and after six months of treatment. Electroencephalogram (EEG) to exclude epilepsy will be performed before and after six months of treatment.
Detailed Description
Participants will be screened by the PI, a specialist neurologist. For those passing screening, license for Cannabis will be obtained at MOH.
Participants will pass tests such as ADOS (communication skills) and Wechsler (IQ), parents will fill questionnaires.
Treatment will start in a titration mode till improvement in some parameters is seen or till treatment failure decision is made.
Participants will be called for a check-up by mid-time (after 3 months) and their parents will fill questionnaires.
Participants will be called for a last check-up after 6 months from treatment beginning and pass again ADOS and Wechsler tests. Parents will fill questionnaires.
Secondary purposes of the trial:
To detect side-effects To assess treatment failure To assess treatment effect on sleep, motor restlessness and behavior. To examine treatment effect on hormonal profile
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Autism Spectrum Disorder
Keywords
Autism, Cannabis, co-morbid symptoms, ASD, Cannabidiol
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
128 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Seach CBD:THC 20:1 cannabis oil
Arm Type
Active Comparator
Arm Description
cannabis oil containing CBD:THC ratio of 20:1. plant material is grown by Seach LTD and oil manufactured by Nextar Pharma LTD.
Arm Title
Candoc CBD:THC 20:1 cannabis oil
Arm Type
Active Comparator
Arm Description
cannabis oil containing CBD:THC ratio of 20:1. plant material is grown by Candoc LTD and oil manufactured by Panaxia LTD.
Intervention Type
Drug
Intervention Name(s)
Cannabis oil
Intervention Description
Cannabis oil 20:1 CBD:THC ratio
Primary Outcome Measure Information:
Title
Cannabinoids levels change
Description
To compare CBD, THC their and metabolites blood levels before and after intervention
Time Frame
3 months
Title
Changes in attention span
Description
To characterize the effect of medical cannabis treatment on the attention span using Conners teacher questionnaires. Significant change is defined as a change of 10% in questionnaire score between baseline and 6 months.
Time Frame
6 months
Title
Changes in cognitive level
Description
To examine the effect of cannabis treatment on cognitive level using part of Wechsler test. Significant change is defined as a change of 10% in questionnaire score between baseline and 6 months.
Time Frame
6 months
Title
Comparison of efficacy between two different cannabis oil products
Description
To compare efficacy of medical cannabis products with the same CBD: THC ratio in terms of communication skills using ADOS test. Significant change is defined as a change of 10% in raw questionnaire score between baseline and 6 months.
Time Frame
6 months
Title
Changes in adaptive behavior
Description
To examine the effect of cannabis treatment on adaptive behavior as per ADOS test. Significant change is defined as a change of 10% in raw questionnaire score between baseline and 6 months.
Time Frame
6 months
Title
Changes in violent behavior
Description
To examine the effect of cannabis treatment on violent behavior as per specific trial-designed questionnaire. Significant change is defined as a change of 10% in questionnaire score between baseline and 6 months.
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Side effects
Description
To identify side effects as per parents report in a specific trial-designed questionnaire. Significant change is defined as a change of 10% in new side effects as examined by questionnaire score between baseline and 6 months.
Time Frame
6 months
Title
Therapeutic failure
Description
To identify therapeutic failure reasons as per Professional expert opinion. Significant reason is defined as reason that will effect at least 20% of therapeutic failure cases.
Time Frame
6 months
Title
Changes in sleep problems
Description
To examine whether high concentration CBD cannabis oil is effective in improving sleep as per Sleep questionnaire. Significant change is defined as a change of 10% in raw questionnaire score between baseline and 6 months.
Time Frame
6 months
Title
Changes in eating problems
Description
To examine whether high concentration CBD cannabis oil is effective in improving eating as per eating questionnaire. Significant change is defined as a change of 10% in raw questionnaire score between baseline and 6 months.
Time Frame
6 months
Title
Changes in hormonal profile
Description
To compare hormonal profile measured as per by Hospital Lab SOP before and during treatment. measured hormones are: TSH, FT4, 17OH-testosterone, LH, prolactine. Significant change is defined as a clinically significant diversion from lab defined normal ranges, according to age and sex, between baseline and 3 months.
Time Frame
3 months
Title
Changes in biochemical parameters
Description
To compare liver enzymes measured as per by Hospital Lab SOP before and during treatment. Measured enzymes are: ALT, AST, GGT, Bilirubin. Significant change is defined as a clinicaly significant diversion (more than twice the Upper Limit of Noraml for each enzyme) from lab defined normal ranges, between baseline and 3 months.
Time Frame
3 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
5 Years
Maximum Age & Unit of Time
25 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria
diagnosed with ASD by DSM
IQ below 70. The investigator can include patients with IQ above 70 if they have significant ASD or comorbid symptoms.
With significant behavior problems in for at least 6 months before recruitment
Exclusion Criteria:
Epilepsy with clinical symptoms
Current or previous treatment with cannabis
Genetic disorder that can cause ASD symptoms
Metabolic disorder
immunologic disorder
liver cancer
Participants who, in the researcher's opinion, will not cooperate in the various research procedures
Women which are pregnant or breastfeeding.
Psychosis or schizophrenia or past or present schizoaffective disorder, in first-degree relatives
History of substance abuse or abuse (including cannabis use disorder or alcohol addiction) in first-degree relatives
Hypersensitivity to coconut oil / palm oil
Facility Information:
Facility Name
Assaf Harofeh Medical Center
City
Zerifin
ZIP/Postal Code
70300
Country
Israel
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
the study protocol to be sahared upon request
IPD Sharing Time Frame
during the duration of the trial
IPD Sharing Access Criteria
for interested colleagues
Citations:
PubMed Identifier
25667194
Citation
Iseger TA, Bossong MG. A systematic review of the antipsychotic properties of cannabidiol in humans. Schizophr Res. 2015 Mar;162(1-3):153-61. doi: 10.1016/j.schres.2015.01.033. Epub 2015 Feb 7.
Results Reference
background
PubMed Identifier
26103030
Citation
Whiting PF, Wolff RF, Deshpande S, Di Nisio M, Duffy S, Hernandez AV, Keurentjes JC, Lang S, Misso K, Ryder S, Schmidlkofer S, Westwood M, Kleijnen J. Cannabinoids for Medical Use: A Systematic Review and Meta-analysis. JAMA. 2015 Jun 23-30;313(24):2456-73. doi: 10.1001/jama.2015.6358. Erratum In: JAMA. 2015 Aug 4;314(5):520. JAMA. 2015 Aug 25;314(8):837. JAMA. 2015 Dec 1;314(21):2308. JAMA. 2016 Apr 12;315(14):1522.
Results Reference
background
PubMed Identifier
30687090
Citation
Barchel D, Stolar O, De-Haan T, Ziv-Baran T, Saban N, Fuchs DO, Koren G, Berkovitch M. Oral Cannabidiol Use in Children With Autism Spectrum Disorder to Treat Related Symptoms and Co-morbidities. Front Pharmacol. 2019 Jan 9;9:1521. doi: 10.3389/fphar.2018.01521. eCollection 2018.
Results Reference
background
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The Effects of Medical Cannabis in Children With Autistic Spectrum Disorder
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