This phase II trial compares the effectiveness of full spectrum cannabidiol (CBD) (fsCBD) to broad spectrum CBD (bsCBD) to placebo for improving pain, mood, sleep, cognitive function, and quality of life in patients who are receiving or have received treatment for solid cancers. Problems with pain, sleep, and mood are common among individuals diagnosed with cancer, and many are turning to cannabis (marijuana) for symptom relief/palliative care. Cannabis may prove less harmful/more beneficial than other palliative care options like opiate medications, and may reduce the use of multiple drugs. CBD is derived from the same plant family as marijuana but is not associated with a “high” or mind-altering effect and is not habit-forming. Delta-9-tetrahydrocannabinol (THC) is a metabolite of cannabis that produces the "high" often associated with marijuana. There is evidence that CBD and THC alone and in combination with one another have varying levels of effectiveness in improving sleep, anxiety, and pain outcomes. fsCBD contains both CBD and THC while bsCBD contains only CBD. This study evaluates whether fsCBD or bsCBD is more effective at improving pain, mood, sleep, cognitive function, and quality of life in patients with cancer.
Additional locations may be listed on ClinicalTrials.gov for NCT06266611.
Locations matching your search criteria
United States
Colorado
Boulder
University of Colorado – BoulderStatus: Active
Contact: Angela Bryan
Phone: 303-492-9549
Denver
University of ColoradoStatus: Active
Contact: Angela Bryan
Phone: 303-492-9549
PRIMARY OBJECTIVES:
I. Compare effects of 8 weeks of use of a daily dose of cannabis (200mg CBD/4mg THC [fsCBD] or 200mg CBD [bsCBD]) versus placebo on pain, mood, sleep, subjective cognitive function, and quality of life.
II. Compare effects of fsCBD and bsCBD versus placebo on acute changes one and two hours after use in beneficial (reductions in pain intensity, mood) versus potentially harmful (subjective “high,” objective cognitive function) outcomes.
SECONDARY OBJECTIVE:
I. Examine polypharmacy in cancer survivors by testing effects of fsCBD and bsCBD relative to placebo on use of pain, sleep, and psychiatric medications over the course of the trial.
OUTLINE: Patients are randomized to 1 of 3 arms.
ARM I: Patients receive fsCBD orally (PO) twice daily (BID) for 8 weeks. Patients also undergo collection of blood samples and wear a heart rate monitor on study.
ARM II: Patients receive bsCBD PO BID for 8 weeks. Patients also undergo collection of blood samples and wear a heart rate monitor on study.
ARM III: Patients receive placebo (hemp seed oil) PO BID for 8 weeks. Patients also undergo collection of blood samples and wear a heart rate monitor on study.
After completion of study treatment, patients are followed for up to 30 days.
Trial PhasePhase II
Trial Typesupportive care
Lead OrganizationUniversity of Colorado – Boulder
Principal InvestigatorAngela Bryan