- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04982965
Brain Mechanisms Supporting Cannabis-induced Pain Relief
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Chronic low back pain is one of the most common causes of pain and disability in adults. Unfortunately, treatments that can directly reduce chronic low back pain remain limited. Cannabis has shown promise for pain relief, but researchers do not yet fully understand how it affects the brain or reduces pain in people with chronic pain.
The purpose of this study is to examine how inhaled (vaporized, not smoked) cannabis affects pain responses and brain activity in adults with chronic low back pain. Researchers will compare the effects of cannabis containing tetrahydrocannabinol (THC) to a placebo cannabis containing 0% THC.
This study involves one visit to the Keck Center for Functional MRI at UC San Diego. Participants will complete screening procedures, questionnaires, and pain testing using heat stimulation applied to the calf. Participants will be trained to rate their pain intensity and unpleasantness. A straight leg raise maneuver will also be performed to assess low back pain and any pain radiating down the leg.
Participants will inhale either THC-containing cannabis or placebo cannabis (no THC) using a vaporization device under study staff supervision. Brain imaging, heat pain testing, leg raise assessments, and pain ratings will be collected before and after cannabis administration to evaluate changes in pain processing and brain activity. Researchers will also assess self-reported pain, mood, sleep, stress, and cannabis-related effects using standardized questionnaires.
This study may improve understanding of how cannabis influences the brain and pain systems in people with chronic low back pain, and findings may help support the development of improved treatments for chronic pain.
Study Type
Enrollment (Estimated)
Phase
- Early Phase 1
Contacts and Locations
Study Contact
- Name: Madelynn Meredith, BS
- Phone Number: 619-431-1850
- Email: mameredith@health.ucsd.edu
Study Contact Backup
- Name: Yasmeen Esshaki, MA
- Phone Number: 619-786-0375
- Email: yesshaki@health.ucsd.edu
Study Locations
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California
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La Jolla, California, United States, 92093
- Recruiting
- Center for Functional MRI - W.M.Keck Building
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Principal Investigator:
- Fadel Zeidan, PhD
-
Contact:
- Madelynn Meredith, BS
- Phone Number: 619-431-1850
- Email: mameredith@health.ucsd.edu
-
Contact:
- Yasmeen Esshaki, MA
- Phone Number: 619-786-0375
- Email: yesshaki@health.ucsd.edu
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Between 21-65 years old
- Currently 30 days cannabis free
- Lower back pain for three months or more
- Are not taking opioids
- If female and of a child bearing potential age, are not pregnant or nursing mothers
- Do not have mental or neurological conditions inhibiting sensory/motor functions
- Do not have a lifetime history of dependence on cannabis
- Do not have a lifetime history of DSM-IV schizophrenia, bipolar disorder, panic disorder, or psychosis
- Prior THC-containing cannabis experience within the past two years
- Agrees not to use cannabis outside of the study during participation in the study
- Agrees not to use opioids or barbiturates during participation in the study
- Agrees not to drive a motor vehicle within 4 hours following last use of inhaled cannabis during participation in the study
Exclusion Criteria:
- 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
- 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
- Any 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
- Overt sensitivity to thermal stimulation
- Resting blood pressure > 140/90
- Resting heart rate > 100 beats/minute
- Prisoner
- Institutionalized
- Claustrophobia
- MRI contraindications
- Participation in any new (within 2 weeks prior or any time after enrollment) pain management procedures during the study period
- Known history of vasovagal fainting, syncope, or severe adverse reactions associated with blood draws or needle procedures
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Active THC
Participants will be administered 400mg of vaporized cannabis (5.1%) before pain testing and fMRI.
|
400 mg of vaporized and inhaled active cannabis (5.1%)
|
|
Placebo Comparator: Placebo THC
Participants will be administered 400mg of vaporized cannabis (<.1%) before pain testing and fMRI.
|
400 mg of vaporized and inhaled placebo cannabis (<.1%)
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Cerebral Blood Flow (CBF)
Time Frame: All data will be collected at the single study session (Day 1).
|
Changes in brain blood flow and oxygen levels will be measured using non-invasive MRI-based brain imaging methods.
These scans will assess how much blood is reaching brain tissue and how oxygen levels in the brain change over time.
|
All data will be collected at the single study session (Day 1).
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pain Ratings
Time Frame: All data will be collected at the single study session (Day 1).
|
Pain ratings will be assessed in response to noxious heat stimulation.
Pain intensity and pain unpleasantness will be measured using a 0-10 Visual Analog Scale (VAS), where 0 indicates "no pain" and 10 indicates "most intense imaginable pain" or "most unpleasant imaginable pain."
Higher scores indicate greater pain intensity or unpleasantness.
Subjective response to cannabis will be assessed using a 0-10 Numeric Rating Scale (NRS), with higher scores indicating greater subjective effects.
|
All data will be collected at the single study session (Day 1).
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Neurochemical Metabolites
Time Frame: All data will be collected at the single study session (Day 1).
|
We will use a specialized, non-invasive brain scan called proton magnetic resonance spectroscopy (1H-MRS) to measure certain brain chemicals linked to pain processing, including glutamate, GABA, and myo-inositol.
The scan uses radiofrequency signals (sim
|
All data will be collected at the single study session (Day 1).
|
|
Respiration Rate
Time Frame: All data will be collected at the single study session (Day 1).
|
Changes in breathing rate may be associated with pain relief and improved well-being.
Breathing rate will be monitored continuously in real time to ensure accurate data collection.
|
All data will be collected at the single study session (Day 1).
|
|
THC Concentrations
Time Frame: All data will be collected at the single study session (Day 1).
|
THC concentrations will be measured to evaluate the relationship between THC levels and pain relief.
|
All data will be collected at the single study session (Day 1).
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Pain
- Neurologic Manifestations
- Bone Diseases
- Musculoskeletal Diseases
- Nervous System Diseases
- Mental Disorders
- Neuromuscular Diseases
- Peripheral Nervous System Diseases
- Spinal Diseases
- Substance-Related Disorders
- Chemically-Induced Disorders
- Neuralgia
- Mononeuropathies
- Sciatic Neuropathy
- Pathological Conditions, Signs and Symptoms
- Signs and Symptoms
- Back Pain
- Radiculopathy
- Marijuana Abuse
- Low Back Pain
- Intervertebral Disc Degeneration
- Sciatica
Other Study ID Numbers
- 200011
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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