Phase
Condition
Diabetic Foot Ulcers
Diabetic Kidney Disease
Diabetic Neuropathy
Treatment
Cannabidiol (CBD) powder formulation
Matching Placebo Cannabidiol (CBD) powder formulation
Clinical Study ID
Ages > 18 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
18 years of age and older
Weight more than 110 pounds
Have a Body Mass Index greater than or equal to 25 kilograms/squared meters
Free of gastrointestinal or metabolic diseases
Sedentary (less than 150 minutes of moderate-intensity exercise per week during theprevious 3 months)
Exclusion
Exclusion Criteria:
Less than 18 years of age
Pregnant or breastfeeding
Have known food allergies
Have been diagnosed with any autoimmune disorders or with compromised immunefunction
Celiac disease
Inflammatory bowel diseases
Gastrointestinal cancers
Diabetes
Human Immunodeficiency Virus
Adverse reaction to ingesting CBD oils, or CBD containing food products
Taking any of the following medications will be excluded as these may have negativeinteractions with CBD:
steroids,
3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors,
calcium channel blockers,
antihistamines,
human immunodeficiency virus antivirals
immune modulators,
benzodiazepines,
antiarrythmics,
antibiotics,
anesthetics,
antipsychotics,
antidepressants,
anti-epileptics,
beta blockers,
coumadin (warfarin),
proton pump inhibitors,
non-steroidal anti-inflammatory drugs,
angiotension II blockers,
oral hypoglycemic agents,
sulfonylureas.
Study Design
Study Description
Connect with a study center
Colorado State University, Dept. of Health and Exercise Science
Fort Collins, Colorado 80523-1582
United StatesSite Not Available

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