Evaluation of a Specific Transdermal Cannabidiol Product for Chronic Musculoskeletal Joint Pain. (CBD001)
Primary Purpose
Musculoskeletal Joint Pain
Status
Withdrawn
Phase
Phase 1
Locations
Study Type
Interventional
Intervention
Cannabidiol
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Musculoskeletal Joint Pain
Eligibility Criteria
Inclusion Criteria
- Diagnosis of chronic musculoskeletal joint pain (arthritis, traumatic arthritis, osteoarthritis)
- Adults ages 18 and over.
- Medically stable without significant medical illness that would preclude treatment with either pharmacologic agent.
- Have a safe, stable, living environment.
Exclusion Criteria
- Unable to consent for research project.
- Individuals less than 18 years of age.
- Individuals with rheumatoid or other autoimmune types of arthritis.
- Individuals diagnosed with SUD especially cannabis, as this may confound results.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Placebo Comparator
Experimental
Arm Label
Placebo Group
Active Group
Arm Description
Does not get active topical CBD. Instead, gets an identical placebo-containing topical agent.
Does get active topic CBD.
Outcomes
Primary Outcome Measures
Change in PGI-S
Patient Global Impression of Severity Scale from 1 to 7 with higher scores indicating worse condition
Change in PGI-C
Patient Global Impression of Change Scale from 1 to 7 with higher scores indicating worse condition
Change in QOLS
Quality of Life Scale Scale from 16 to 112, with higher scores indicating better condition
Secondary Outcome Measures
Full Information
NCT ID
NCT05002114
First Posted
August 2, 2021
Last Updated
June 30, 2022
Sponsor
Louisiana State University Health Sciences Center Shreveport
1. Study Identification
Unique Protocol Identification Number
NCT05002114
Brief Title
Evaluation of a Specific Transdermal Cannabidiol Product for Chronic Musculoskeletal Joint Pain.
Acronym
CBD001
Official Title
Evaluation of a Specific Transdermal Cannabidiol Product for Chronic Musculoskeletal Joint Pain.
Study Type
Interventional
2. Study Status
Record Verification Date
June 2022
Overall Recruitment Status
Withdrawn
Why Stopped
there were issues with the primary study material that prohibited continuation at this time
Study Start Date
January 2023 (Anticipated)
Primary Completion Date
January 2023 (Anticipated)
Study Completion Date
January 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Louisiana State University Health Sciences Center Shreveport
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Double-blind, randomized into two arms (TC and TP): patients get either topical cannabidiol or topical placebo up to three times daily. Inclusion criteria will be chronic joint pain with intent to treat or currently treated with opioids. Exclusion criteria will include current cannabis use, severe medical illness or lacking in capacity to be involved in study. TC and TP will be prescribed for use TID in predefined dosages and quantities.
Detailed Description
Introduction and Rationale
Currently, the opioid epidemic is a public health crisis. Use of opioids for chronic pain are a large component of this crisis. If alternative means can be developed to treat chronic pain that can replace the use of opioid-based treatments, this can improve clinical outcomes and quality of life.
Arthritis and musculoskeletal pain are often chronic conditions that cause significant morbidity. Historically, one study estimated that the lifetime incidence is as high as 47% for osteoarthritis over the lifespan, increasing with age and also increasing to 60% with a body mass index over than 30. In our society today with over 50% of the population suffering from obesity, this is a significant problem.
While cannabis products have been referenced for treating numerous medical issues including a number of pain-related conditions, it has only been recently that mechanisms outside the central nervous system have been recognized. There is very little published in regards to the use of cannabidiol (CBD) in the treatment of arthritic pain, and even less on the topical application of CBD products in its use in this manner. Two previous studies demonstrated the efficacy of a local/transdermal application of CBD in rodent models of arthritis. Activity at the TRPV2 receptor is one possible mechanism for this putative mechanism. Another possible interaction is at the GPR55 receptor.
The earliest known references to the medicinal properties of cannabis can be found in the "Shennong Ben Cao Jing", which describe Chinese uses of herbal remedies from as early as 2700 BC. In later compilations of this work, cannabis is described as being utilized for the treatment of pain and inflammation. Since that time, cannabis has been used world-wide both medicinally and for recreational purposes. It has only been a recent development (within the past 100 years) that public health regulations have prohibited the use of cannabis products.
However, problems do exist with the use of CBD products. The FDA has issued numerous letters warning manufacturers of CBD products about false advertising and/or illegal marketing of CBD for unapproved uses to treat disorders such as Alzheimer's disease. In addition, prior evaluations of products containing CBD found that 69% were mislabeled in regards to the contents provided on the product labels. Given these matters, it is our intent to evaluate the efficacy of a topical CBD (TC) preparation in improving clinical outcomes in patients with chronic musculoskeletal joint pain. Specifically the investigators wish to establish the efficacy of TC, a product specifically formulated for topical application at pre-defined dosages.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Musculoskeletal Joint Pain
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Model Description
double-blind, randomized, placebo-controlled.
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
double-blind, randomized, placebo-controlled.
Allocation
Randomized
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Placebo Group
Arm Type
Placebo Comparator
Arm Description
Does not get active topical CBD. Instead, gets an identical placebo-containing topical agent.
Arm Title
Active Group
Arm Type
Experimental
Arm Description
Does get active topic CBD.
Intervention Type
Drug
Intervention Name(s)
Cannabidiol
Intervention Description
Topical CBD cream - special formulation
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
Not the drug
Primary Outcome Measure Information:
Title
Change in PGI-S
Description
Patient Global Impression of Severity Scale from 1 to 7 with higher scores indicating worse condition
Time Frame
Two time points, before treatment and after 4 weeks.
Title
Change in PGI-C
Description
Patient Global Impression of Change Scale from 1 to 7 with higher scores indicating worse condition
Time Frame
Two time points, before treatment and after 4 weeks.
Title
Change in QOLS
Description
Quality of Life Scale Scale from 16 to 112, with higher scores indicating better condition
Time Frame
Two time points, before treatment and after 4 weeks.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria
Diagnosis of chronic musculoskeletal joint pain (arthritis, traumatic arthritis, osteoarthritis)
Adults ages 18 and over.
Medically stable without significant medical illness that would preclude treatment with either pharmacologic agent.
Have a safe, stable, living environment.
Exclusion Criteria
Unable to consent for research project.
Individuals less than 18 years of age.
Individuals with rheumatoid or other autoimmune types of arthritis.
Individuals diagnosed with SUD especially cannabis, as this may confound results.
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Evaluation of a Specific Transdermal Cannabidiol Product for Chronic Musculoskeletal Joint Pain.
We'll reach out to this number within 24 hrs