Cannabigerol for Psychological and Physiological Effects
(CBG Trial)
Trial Summary
What is the purpose of this trial?
The purpose of this study is to examine the acute effects of cannabigerol (CBG) on various psychological (e.g., anxiety, stress, mood, memory, impairment, intoxication, side effects) and physiological (blood pressure, cortisol, heart rate variability, electrodermal activity, pain tolerance, temperature) outcomes. Further, potential side effects of CBG (sleepiness/fatigue, dry mouth/eyes, increased appetite, and dizziness nausea) will be assessed. As such, the study is focused on better understanding some of the potentially beneficial and detrimental effects of CBG on humans.
Will I have to stop taking my current medications?
The trial information does not specify whether you need to stop taking your current medications. It's best to discuss this with the trial coordinators or your doctor.
What evidence supports the effectiveness of the drug Cannabigerol (CBG) for psychological and physiological effects?
Research suggests that CBG may help with anxiety, chronic pain, depression, and insomnia, with many users reporting improvements over conventional medicines. It also shows potential for treating neurological disorders and inflammatory conditions, although more studies are needed to confirm these benefits.12345
Is Cannabigerol (CBG) safe for human use?
How is the drug Cannabigerol (CBG) unique compared to other treatments?
Cannabigerol (CBG) is unique because it interacts with specific receptors in the body differently than other cannabinoids like THC and CBD, showing potential for treating neurological disorders and inflammation without psychoactive effects. It is also being explored for its anti-anxiety, neuroprotective, and pain-relieving properties, making it a promising option for conditions that require a multi-faceted approach.12345
Eligibility Criteria
This trial is for individuals interested in participating in a study to assess the effects of cannabigerol (CBG), a compound found in cannabis. There are no specific conditions listed, so participants may be from the general population.Inclusion Criteria
Exclusion Criteria
Timeline
Screening
Participants are screened for eligibility to participate in the trial
Baseline Assessment and CBG/Placebo Administration
Participants undergo baseline assessments and are administered either CBG or placebo
Testing Session 1
Participants complete various psychological and physiological assessments after CBG/placebo administration
Washout Period
Participants undergo a one-week washout period before the second testing session
Testing Session 2
Participants complete a second round of assessments with the opposite product (CBG or placebo)
Follow-up
Participants are monitored for any delayed effects or side effects post-study
Treatment Details
Interventions
- Cannabigerol (CBG)
Find a Clinic Near You
Who Is Running the Clinical Trial?
Washington State University
Lead Sponsor