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NCT Number: NCT06393101

The Effects and Mechanisms of a High CBD Cannabis Extract (BRC-002) for the Treatment of Pain and Health in Complex Regional Pain Syndrome

The aim of this trial is to determine the potential effects and mechanisms of cannabinoid-induced pain relief in complex regional pain syndrome (CRPS). Multiple psychophysical approaches will be conducted in conjunction with psychological and inflammatory marker testing to determine if and how cannabinoids produce stabilized improvement in CRPS-related pain and comorbidities.

The trial consisted of a pre-treatment screening period, six-week treatment period and a two-week follow-up.

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Key information

Age range

21 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Altman Clinical and Translational Research Institute, La Jolla, California, United States

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About this study

Complex Regional Pain Syndrome (CRPS) is a debilitating and perplexing chronic pain condition that produces incalculable suffering to millions of individuals worldwide. The enigmatic nature of CRPS has left it difficult to treat. CRPS is characterized by a constellation of pain, sensory, autonomic, and motor symptoms that is difficult to pinpoint the source of injury/inflammation. Although unclear, a common cause of CRPS are radial fractures that demonstrate aberrant processing 4-6 weeks after injury.

The aim of this trial is to determine the potential effects and mechanisms of cannabinoid-induced pain relief in complex regional pain syndrome (CRPS). Multiple psychophysical approaches will be conducted in conjunction with psychological and inflammatory marker testing to determine if and how cannabinoids produce stabilized improvement in CRPS-related pain and comorbidities.

The trial consisted of a pre-treatment screening period, six-week treatment period and a two-week follow-up.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Provision of signed and dated informed consent form.
  • Are between 21-75 years old
  • Ability to communicate in English
  • Volunteers with no previous medical history (e.g., cardiac or pulmonary disease)
  • Are not currently using any type of cannabis, including hemp or CBD
  • Currently 30 days cannabis free
  • Participants with ongoing CRPS [Type 1 or Type 2)] for at least 3 months prior to participation (medical record confirmed)
  • Agrees not to use cannabis, including hemp or CBD, outside of the study during participation in the study
  • Agrees not to use opioids or barbiturates during participation in the study

Exclusion criteria

  • Fail cannabis screening
  • Active pulmonary disease
  • Allergy or past adverse effects or negative past experiences from cannabis
  • Positive urine drug test for THC, barbiturates, opioids, oxycodone, or methadone prior to study session 1 or session 2
  • Any significant illness, including cardiovascular disease, diabetes, renal and liver disease
  • Any current or history of an immunocompromising disease or condition (such as lupus, psoriasis, multiple sclerosis, etc.)
  • Any current or history of neurologic conditions, including Parkinson disease, dementia, cognitive impairment, history of seizure disorder, and history of traumatic brain injury/head injury
  • Participant meets DSM-V criteria for current major psychiatric illness, such as bipolar disorder, major depression, psychosis, substance use disorder, or schizophrenia
  • Any current or history of suicidal ideation or attempt
  • Patients with clinically significant laboratory abnormalities

Treatment and study plan

BRC-002

Drug

BRC-002 is a non-scheduled cannabidiolic (CBD) formulation (<.3% THC). The cannabinoids in BRC-002 are naturally biosynthesized within the Cannabis sativa L. plant as acidic forms of CBD (cannabidiolic acid; CBDA), THC (tetrahydrocannabinolic acid; THCA) and other minor cannabinoids.

BRC-002 Placebo

Drug

Oral solution of mono-, di-, and triglycerides

Primary outcomes

  1. Change in complex regional pain syndrome pain and heat pain measured with VAS

    Time frame: Day 1 - Day 42

    Change from baseline in pain intensity and unpleasantness ratings using an 11-point Visual Analog Scale in response to heat and ongoing CRPS pain

Secondary outcomes

  1. Pain Inventory Measure

    Time frame: Day 1 - Day 42

    Change from baseline in The Brief Pain Inventory

  2. Depression Measure

    Time frame: Day 1 - Day 42

    Change from baseline in Beck Depression

  3. Sleep Measure

    Time frame: Day 1 - Day 42

    Change from baseline in Pittsburgh Sleep Quality Index

  4. Interleukin 6

    Time frame: Day 1 - Day 42

    Change from baseline in Interleukin 6

Study contacts

Contact information is provided by the study sponsor or research team.

Fadel Zeidan, PhD

CONTACT

[email protected]

858-246-8341

Yasmeen Esshaki, MS

CONTACT

[email protected]

858-246-8341

Sponsors and collaborators

Lead sponsor

University of California, San Diego

Other

Registry information

Official study title

A Randomized, Double-blind, Placebo-controlled Study to Investigate the Effects and Mechanisms of a High CBD Cannabis Extract (BRC-002) for the Treatment of Pain and Health in Complex Regional Pain Syndrome

Important dates

Study start
2024
Primary completion
2029
Study completion
2029
First posted
May 1, 2024
Registry last updated
Jun 7, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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