Mechanisms of Cannabidiol in Persons With MS: the Role of Sleep and Pain Phenotype
Study Details
Study Description
Brief Summary
The purpose of this research study is to compare the effects of cannabidiol (CBD), tetrahydrocannabinol (THC), or both, on sleep and pain in persons with multiple sclerosis (MS). Little is known about how CBD and/or THC may help sleep, reduce pain, or perhaps even treat pain through better sleep.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 2 |
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Cannabidiol (CBD) Epidiolex® doses will be 0.5 mL twice daily during the first seven days of active treatment and 1 mL twice daily (b.i.d.) for the remaining days of treatment. PLUS Placebo Tetrahydrocannabinol (TCH) capsules which contain no active ingredients. Matching placebo capsules will be taken twice per day in the same schedule and manner as active dronabinol. |
Drug: Cannabidiol (CBD)
Epidiolex® doses will be 0.5 mL twice daily during the first seven days of active treatment and 1 mL twice daily (b.i.d.) for the remaining treatment.
Other Names:
Drug: Placebo THC
Placebo capsules will be taken twice per day in the same schedule and manner as active dronabinol.
|
| Active Comparator: Tetrahydrocannabinol (THC) The drug dose will be 2.5 mg b.i.d. during the first seven days of active treatment, and 5 mg b.i.d. for the following days of active treatment. PLUS Placebo CBD (A matching placebo oral solution to Epidiolex® will be used that consists of all of the excipients in the active solution without the cannabidiol component). The placebo will be dosed in the same schedule and manner as active Epidiolex®. |
Drug: Tetrahydrocannabinol (THC)
The drug dose will be 2.5 mg b.i.d. during the first 7 days of active treatment, and 5 mg b.i.d. for the following treatment.
Other Names:
Drug: Placebo CBD
Placebo solution will be taken twice per day, using the same dosing regimen as described for Epidiolex®.
|
| Active Comparator: CBD + THC
|
Drug: Cannabidiol (CBD)
Epidiolex® doses will be 0.5 mL twice daily during the first seven days of active treatment and 1 mL twice daily (b.i.d.) for the remaining treatment.
Other Names:
Drug: Tetrahydrocannabinol (THC)
The drug dose will be 2.5 mg b.i.d. during the first 7 days of active treatment, and 5 mg b.i.d. for the following treatment.
Other Names:
|
| Placebo Comparator: Placebo CBD + Placebo THC
|
Drug: Placebo CBD
Placebo solution will be taken twice per day, using the same dosing regimen as described for Epidiolex®.
Drug: Placebo THC
Placebo capsules will be taken twice per day in the same schedule and manner as active dronabinol.
|
Outcome Measures
Primary Outcome Measures
- Mean change in sleep bout length [Baseline, 12 weeks]
Measured with in-laboratory polysomnography, reported as average length of continuous bouts of sleep, for each sleep stage and total sleep (in minutes).
- Change in Walsh Spectral Entropy [Baseline, 12 weeks]
Measured with in-laboratory polysomnography, computed from EEG sleep stage data to quantify hypnogram regularity (dimensionless, values range from 0-1)
- Change in Transition Entropy [Baseline, 12 weeks]
Measured with in-laboratory polysomnography. Entropy measure computed from sleep stage transition matrix that quantifies hypnogram regularity (dimensionless, values range from 0-1)
- Change of center of activity [Baseline, 12 weeks]
Measured with in-laboratory polysomnography. Weighted mean temporal location over the night of all 30 second epochs scored as N3 and Rapid eye movement (REM) sleep
- Change in sleep rhythmicity [Baseline, 12 weeks]
Measured by actigraphy. Probability of being in the same sleep/wake state 24h apart
- Change in sleep regularity [Baseline, 12 weeks]
Measured by actigraphy in hours.
- Change in sleep continuity and duration [Baseline, 12 weeks]
Measured by actigraphy in minutes to obtain time in wakefulness after sleep onset (WASO) and total sleep time.
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Patients with clinically definite MS (those who are on a disease modifying therapy must be on a stable dose without evidence of liver toxicity for at least 3 months);
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Presence of chronic pain defined as moderate to severe pain for at least 3 months, based on a 0-10 numeric rating scale (NRS);
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Willingness to maintain stable analgesic regimen during study period;
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Recent serum aspartate transaminase, alanine transaminase, and bilirubin testing within 90 days of screening;
Exclusion Criteria:
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Current shift work sleep disorder, or narcolepsy diagnosed with polysomnography and multiple sleep latency test;
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History of MS relapse within the last 30 days prior to screening (participants will be considered eligible after the 30-day window);
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Pain due to cancer;
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Pregnancy or breastfeeding;
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Current cannabinoid use (participants may be reconsidered for inclusion after 30- day washout) and/or unwillingness to abstain from cannabinoids in any form from 30 days prior to the study of the study drugs and until the last follow up phone call at the end of the study (30 - 37 days after taking the last dose of the study drug).
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Unwillingness to use contraception from screening until the end of drug treatment
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Current suicidal ideation (SI) with intent and/or plan; these individuals will be assessed by a study psychologist and referred for urgent mental health treatment as indicated;
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Current severe depression as indicated by a Patient Health Questionnaire (PHQ)-9 score of ≥ 17 that includes indicators of significant depressed mood (sum of items #1 and #2 ≥ 5).
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History of mania or schizophrenia diagnosis
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Known hypersensitivity to cannabinoids in general, or Epidiolex® or Dronabinol specifically or its excipients (e.g., sesame oil)
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Severe cardiovascular disease (examples: stroke, myocardial infarction, unstable angina, severe coronary artery disease, congestive heart failure, or severe valvular abnormalities)
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History severe hepatic impairment (must have blood alanine aminotransferase (AST) ≤ 2.0x upper limit of normal (ULN), alanine transaminase (ALT) ≤ 2,0x ULN, and bilirubin ≤ 1.5x ULN within the last 90 days (AST, ALT, bilirubin testing will be required within 90 days of screening);
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History of seizure disorder (recurrent, unprovoked seizures not explained by a known reversible cause) or history of certain types of head injury that could cause an increased risk of seizures;
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History of prescription or illicit drug abuse (such as cocaine, amphetamine, methamphetamine, heroin);
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Current risk for alcohol misuse as indicated by a score of ≥ 8 on the Alcohol Use Disorders Identification Test (AUDIT) self-report measure.
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Current warfarin, valproate or clobazam use.
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Current use of known moderate or strong inhibitors of CYP3A4 and CYP2C19 [topical ketoconazole, and temporary (<= 4 week) oral courses of clarithromycin, fluconazole and itraconazole will be allowed].
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Current use of strong inducers of CYP3A4 or CYP2C19 (does not include glucocorticoids or modafinil/armodafinil, which are permitted),
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Current use of moderate or strong inhibitors/inducers of CYP2C9, and narrow therapeutic index drugs (e.g., cyclosporine, amphotericin B).
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Current use of known Sensitive CYP2C19 Substrates, with the exception of some proton pump inhibitors (esomeprazole, omeprazole, and pantoprazole), imipramine, clomipramine, periodic self-limited courses of diazepam (e.g., for MRI sedation) and submaximal doses of some antidepressant class medications (amitriptyline, citalopram, and escitalopram), which will be permitted by the discretion of the treating neurologist principal investigator.
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Refusal to avoid grapefruit or grapefruit products during the study treatment interval.
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Current use of opioids (tramadol permitted).
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Employed as a commercial driver or employed in an occupation that involves extreme heights or use of heavy machinery.
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History of car crashes or near-crashes due to sleepiness.
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Cognitive dysfunction as indicated by >=3 errors on the six-item cognitive screener
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Expanded Disability Status Scale (EDSS) score >=8.0.
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Blood pressure at screening above 180 mmHg systolic and/or 120 mmHg diastolic, or below 90 mmHg systolic and or 60 mmHg diastolic, or history of syncope related to orthostatic hypotension;
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Resting heart rate at screening less than 50 bpm or greater than 100 bpm;
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Any other treatment or medical, neurological, sleep, or psychiatric condition that, in the opinion of the investigators, could affect participant safety or eligibility.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | University of Michigan | Ann Arbor | Michigan | United States | 48109 |
Sponsors and Collaborators
- Tiffany J. Braley, MD, MS
- National Center for Complementary and Integrative Health (NCCIH)
Investigators
- Principal Investigator: Tiffany Braley, University of Michigan
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- HUM00190734
- 1R01AT011341-01