Key Findings: 
Type of Study: 
Study Result:  Inconclusive
Research Location(s): 
Year of Pub: 
Cannabinoids Studied: 
Chemotype: 
Terpenes Studied: 
Receptors Studied: 
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DOSING DETAILS   
Study Dosing Objective:  Effective Dose, Safety Profile
Established Protocol:  Effective dose with adverse effects
Route of Administration: 
Cannabinoid Ratio:  (CBD : CBG)   35 : 50    
Dosage Form:  cannabidiol(CBD; 35 mg) cannabigerol (CBG; 50 mg) beta-caryophyllene (BCP; 25 mg) branched-chain amino acids (BCAAs; 3.8 g) magnesium citrate (420 mg)
Dosing Regimen:  Participants consumed the formulation twice per day
Treatment Duration:  3.5 days
Clinical Relevance:  The tested formulation improved function and reduced interference of delayed onset muscle soreness on daily activities.
Adverse Events:  One adverse event in the active group (diarrhea) and two in the placebo (dry mouth; eye rash/swollen eye).
Citation: