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Clinical Trial Summary

Our proposal objective is to evaluate if state-regulated topical CBD-based products relieve chronic musculoskeletal pain and/or absorb into the bloodstream.


Clinical Trial Description

The goal of this study is to learn more about the analgesic efficacy of state-regulated topical cannabinoid products (creams, lotions, salves, etc) and to determine if these topical products are absorbed systemically and can be detected in blood samples. Given that state-regulated dispensary products cannot be brought onto the university campus, this observational study design utilizes a Mobile Pharmacology Laboratory that will go to study participants' homes. Blood samples and other assessments will taken in the mobile lab prior to use of a topical cannabinoid product and at several time points afterwards (4 hours, 24 hours, and 2 weeks). Participants will also collect microsamples of blood using a small device at home at three time points during the first 2-72 hours after application of the product. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05908552
Study type Observational
Source University of Colorado, Denver
Contact Emily Lindley, PhD
Phone 3037240923
Email CUPainStudies@cuanschutz.edu
Status Not yet recruiting
Phase
Start date July 1, 2023
Completion date August 31, 2024

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