Low Dose of Cannabidiol (CBD) to Treat Mild to Moderate Musculoskeletal Pain

NCT04193631 | Completed Phase 1 DMC

• 1 other identifier: PG-19-00A
• Study Type: interventional
• Target: 16
• Locations: 1 country
• Sites: 1

Brief Summary

The purpose of the study is to evaluate whether Pure Green tablets is a better pain reliever for the treatment of mild to moderate musculoskeletal pain.

Conditions

Musculoskeletal Pain

Keywords

CBD; Cannabidiol; Musculoskeletal Pain; Pain

Outcome Measures

Primary Outcomes (1)

• Impact of Pure Cannabidiol (CBD) tablets on safety in patient's with musculoskeletal pain using a self-reported pain scale score.

  To evaluate the safety and efficacy of Pure Green Cannabidiol (CBD) sublingual tablets for the treatment of musculoskeletal pain by having patients evaluate their Numeric Pain Rating Scale (NPRS) score reported as 0-10 where 0 is no pain and 10 is the worst pain possible.

  1 Day

Secondary Outcomes (1)

• To evaluate efficacy of a low dose of Cannabidiol (CBD) in the treatment of mild to moderate musculoskeletal pain.

  1 Day

Study Arms (1)

Pure Green Tablet

EXPERIMENTAL

A water-soluble sublingual tablet that contains 5 mg of cannabidiol (CBD).

Drug: Cannabidiol (CBD)

Interventions

Cannabidiol (CBD) DRUG

A single dose of Cannabidiol (CBD) when patients experience musculoskeletal pain in the trial.

Pure Green Tablet

Eligibility Criteria

• Age: 21 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Male or female at least 21 years of age;
• Subject has mild to moderate musculoskeletal pain;
• Pain for greater than or equal to 10 days of each month for 3 months prior to study entry for which the pain requires treatment.
• Has an Numeric Pain Rating Scale (NPRS) score of 3 or greater,
• If female, subject is practicing an approved method of birth control throughout the study;
• Subject is willing and able to comply with all protocol-specified requirements;
• Subject is willing to take Pure Green tablets only and will not take any other pain medications,
• Subject is willing to provide his/her written informed consent to participate in the study as stated in the informed consent document.
• Subject is willing to document pain scale scores in a diary.

You may not qualify if:

• Subject has any condition for which the investigator does not feel the participant should be enrolled due to possible safety or compliance issues;
• Subject has received treatment with an investigational drug or therapy within 30 days or 5 half-lives (whichever is longer) prior to Day 1.
• Subject has a known allergy to active or inert ingredients of Pure Green tablets;
• Subject is taking a concomitant medication or treatment that would complicate use or interpretation of the study drug's effects (examples include: Cannabis (marijuana) or any cannabinoid products including Cannabidiol (CBD) or Tetrahydrocannabinol (THC); Any drug or herbal product that influences the endocannabinoid system (ECS));
• Have serious cardiovascular, hepatic, renal, respiratory, or hematologic illness, or other medical or psychiatric condition that, in the opinion of the investigator, would compromise participation or be likely to lead to hospitalization during the course of the study.
• Have a history of recurrent seizures other than febrile seizures.
• Have current or pending disability compensation or litigation issues that may compromise response to treatment, in the opinion of the investigator.
• Have a diagnosis of inflammatory arthritis (that is, rheumatoid arthritis) or an autoimmune disorder (excluding inactive Hashimoto's thyroiditis).
• Use of acupuncture, chiropractic maneuvers, transcutaneous electrical nerve stimulation (TENS), or similar procedures aimed to relieve any kind of pain.
• Patients who are anticipated by the investigator to require use of analgesic agents including but not limited to non-steroidal anti-inflammatory drugs (NSAIDs), acetaminophen/paracetamol, and opioids, or other excluded medication for the duration of the study.
• Are unwilling or unable to comply with the data collection method used to record their patient rated outcome data.

Sponsors & Collaborators

• Pure Green: lead

Study Sites (1)

Dr. Kimless' Clinic

Chadds Ford, Pennsylvania, 19317, United States

Location

Related Publications (4)

• Madden K, van der Hoek N, Chona S, George A, Dalchand T, Baldawi H, Mammen G, Bhandari M. Cannabinoids in the Management of Musculoskeletal Pain: A Critical Review of the Evidence. JBJS Rev. 2018 May;6(5):e7. doi: 10.2106/JBJS.RVW.17.00153. No abstract available.

  PMID: 29787450 BACKGROUND

• Hill KP, Palastro MD, Johnson B, Ditre JW. Cannabis and Pain: A Clinical Review. Cannabis Cannabinoid Res. 2017 May 1;2(1):96-104. doi: 10.1089/can.2017.0017. eCollection 2017.

  PMID: 28861509 BACKGROUND

• Therapeutic Effects of Cannabis and Cannabinoids, National Academies of Sciences, Engineering, and Medicine; Health and Medicine Division; Board on Population Health and Public Health Practice; Committee on the Health Effects of Marijuana: An Evidence Review and Research Agenda. Washington (DC): National Academies Press (US); 2017 Jan 12.

  BACKGROUND

• Ware MA, Wang T, Shapiro S, Collet JP; COMPASS study team. Cannabis for the Management of Pain: Assessment of Safety Study (COMPASS). J Pain. 2015 Dec;16(12):1233-1242. doi: 10.1016/j.jpain.2015.07.014. Epub 2015 Sep 16.

  PMID: 26385201 BACKGROUND

MeSH Terms

Conditions

Musculoskeletal Pain; Pain

Interventions

Cannabidiol

Condition Hierarchy (Ancestors)

Muscular Diseases; Musculoskeletal Diseases; Neurologic Manifestations; Signs and Symptoms; Pathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Cannabinoids; Terpenes; Hydrocarbons; Organic Chemicals

Study Officials

• Debra Kimless, MD

  Chief Medical Officer

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: December 8, 2019
• First Posted: December 10, 2019
• Study Start: December 7, 2019
• Primary Completion: December 9, 2019
• Study Completion: December 9, 2019
• Last Updated: March 24, 2020

Record last verified: 2020-03

Data Sharing

• IPD Sharing: Will not share

Locations

US (1)