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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Withdrawn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
Louisiana State University Health Sciences Center Shreveport
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Musculoskeletal Joint Pain

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria

  1. Diagnosis of chronic musculoskeletal joint pain (arthritis, traumatic arthritis, osteoarthritis)
  2. Adults ages 18 and over.
  3. Medically stable without significant medical illness that would preclude treatment with either pharmacologic agent.
  4. Have a safe, stable, living environment.

Exclusion Criteria

  1. Unable to consent for research project.
  2. Individuals less than 18 years of age.
  3. Individuals with rheumatoid or other autoimmune types of arthritis.
  4. 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

    First Posted
    August 2, 2021
    Last Updated
    June 30, 2022
    Sponsor
    Louisiana State University Health Sciences Center Shreveport
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    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.

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