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Cannabidiol
CBD for Cannabidiol
Phase 1 & 2
Waitlist Available
Led By Godfrey Pearlson, MD
Research Sponsored by Hartford Hospital
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up post drug administration at 3 hours
Summary
This trial is studying CBD, a non-intoxicating cannabis compound, to see if it can help reduce psychosis symptoms in patients with schizophrenia, schizoaffective disorder, or bipolar disorder. CBD works by affecting brain areas involved in mood and perception. Cannabidiol (CBD), a non-psychoactive component of cannabis, shows great promise for the treatment of psychosis and is associated with fewer side effects than conventional antipsychotic drugs.
Who is the study for?
This trial is for adults aged 18-50 with schizophrenia, schizoaffective disorder, or bipolar I disorder with psychotic features, as well as healthy individuals without severe mental illness. Participants must have normal liver function and be able to consent and understand English. Excluded are those allergic to CBD, left-handed individuals (as defined by a specific test), recent substance abusers, those at high risk of suicide or homicide, with certain neurological/medical conditions or on interacting medications.
What is being tested?
The study investigates the effects of CBD versus a placebo on the hippocampus during an fMRI memory task in patients with certain psychiatric disorders compared to healthy controls. It aims to demonstrate whether CBD can engage brain targets related to psychosis and if it has potential antipsychotic properties.
What are the potential side effects?
While not explicitly listed in the provided information, common side effects of CBD may include tiredness, diarrhea, changes in appetite/weight. Since this is a non-intoxicating compound unlike THC from cannabis plants, psychoactive side effects are not expected.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ post drug administration at 3 hours
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~post drug administration at 3 hours
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
CBD dose-response for fMRI Hippocampal BOLD values
Side effects data
From 2014 Phase 2 trial • 50 Patients • NCT018446872%
headache
2%
Blurred Vision
2%
Cold Symptoms
2%
Gastrointestinal Upset
2%
anxiety
100%
80%
60%
40%
20%
0%
Study treatment Arm
Active MJ With 0 mg CBD
Active MJ With 200 mg CBD
Active MJ With 400 mg CBD
Active MJ With 800 mg CBD
Inactive MJ With 0 mg CBD
Inactive MJ With 200 mg CBD
Inactive MJ With 400 mg CBD
Inactive MJ With 800 mg CBD
Trial Design
2Treatment groups
Experimental Treatment
Group I: Patients with psychosisExperimental Treatment2 Interventions
People who are part of a dimensionally-organized psychosis sample spanning several serious mental illness diagnoses including schizophrenia, schizoaffective disorder, or psychotic bipolar I disorder. Eligible participants will be scheduled for two dose visits where they will receive a 600mg CBD dose on one day and a placebo dose on the other day. Doses will be randomized and double-blind. Doses will be administered via oral gel capsules.
Group II: Healthy controlsExperimental Treatment2 Interventions
People who do not have a diagnosis of schizophrenia, schizoaffective disorder, or psychotic bipolar I disorder. Eligible participants will be scheduled for two dose visits where they will receive a 600mg CBD dose on one day and a placebo dose on the other day. Doses will be randomized and double-blind. Doses will be administered via oral gel capsules.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
CBD
2016
Completed Phase 2
~530
Placebo
1995
Completed Phase 3
~2670
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Cannabidiol (CBD) primarily exerts its effects through modulation of the endocannabinoid system, particularly by interacting with cannabinoid receptors (CB1 and CB2) and other neurotransmitter systems. Unlike THC, CBD is non-intoxicating and has been shown to have antipsychotic properties, potentially by opposing the effects of THC.
This is significant for patients as CBD can modulate hippocampal activity, which is crucial for memory and cognitive function. These properties make CBD a promising treatment for conditions like schizophrenia, schizoaffective disorder, and bipolar disorder with psychosis, as it may help alleviate psychotic symptoms without the psychoactive effects associated with THC.
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Logistics
Participation is compensated
You will be compensated for participating in this trial.
Who is running the clinical trial?
Hartford HospitalLead Sponsor
138 Previous Clinical Trials
19,377 Total Patients Enrolled
Yale UniversityOTHER
1,919 Previous Clinical Trials
3,040,335 Total Patients Enrolled
Godfrey Pearlson, MDPrincipal InvestigatorFounding Director Olin Research Center; Professor Yale University
2 Previous Clinical Trials
9 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- You have had an allergic reaction to CBD or products that contain CBD in the past.You strongly prefer to use your left hand for most activities, according to a hand preference test.You have been diagnosed with alcohol or drug abuse or dependence within the past month or three months, as determined by the DSM-IV guidelines.You have thoughts of hurting others and have a plan to do so, making it necessary for you to receive inpatient care instead of outpatient care.You have a serious neurological condition or a severe medical condition that could affect how your brain functions.You have been diagnosed with schizophrenia, schizoaffective disorder, bipolar I disorder with psychotic features, or any other severe mental illness. Or, you are a healthy individual with no diagnosed severe mental illness.
Research Study Groups:
This trial has the following groups:- Group 1: Patients with psychosis
- Group 2: Healthy controls
Awards:
This trial has 0 awards, including:Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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