VA launches major trial of THC and CBD for Veterans' nerve pain
NCT ID NCT05351801
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This phase 2 trial is testing whether cannabis-based medicines—THC, CBD, or a combination—can safely reduce chronic nerve pain in Veterans. 320 participants will receive one of these treatments or a placebo for six weeks. The goal is to see if these options offer better pain relief than current treatments, which often fall short.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- THC (Syndros), CBD (Epidiolex), and THC+CBD (Nabiximols)
- What this could lead to
- If successful, this trial could provide evidence that cannabis-based medicines are a safe and effective option for managing chronic neuropathic pain, especially for Veterans.
- What could go wrong
- This is a mid-stage trial with 320 participants, so results are not definitive. The effects may be modest, and side effects like dizziness or drowsiness are possible. It also focuses on Veterans, so findings may not apply to everyone.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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About 320 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jun 2023
- Expected to finish
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May 2029
An estimate. End dates often move.
- Lead sponsor
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A government agency
The lead sponsor is a US federal agency other than the NIH.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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21 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Able to provide written consent * Veterans 21 years and older at the date of screening * Meet diagnostic criteria for neuropathic pain as defined by the Neuropathic Pain Special Interest Group of the International Association for the Study of Pain (NeuPSIG) * Meet criteria for persistent, high-impact pain criteria. * Presence of allodynia confirmed by one of the screening dynamic brush tests * women of childbearing potential who agree to abide by contraceptive requirements Exclusion Criteria: * Actively engaged in or planning to enter a program of non-pharmacological invasive intervention for pain at the time of enrollment * Peripheral neuropathy is not a primary source of neuropathic pain * Hypersensitivity to THC, CBD, or THC/CBD * Self-report of cannabis use during screening phase confirmed by positive urine toxicology for THC-COOH as measured and resulted at visit 5 before randomization * Unwilling to refrain from using cannabis or cannabis-based products through the entire duration of the study * Diagnosis of DSM-5 Cannabis Use Disorder in the past 6 months * Current DSM-5 diagnosis of cannabis use disorder, substance use disorder or serious psychiatric disorders * Actual change or intent to change is greater than a 20% change (increase or decrease) in any other medication for pain or non-pharmacological treatment from 4 weeks before the screening appointment until completion of study (i.e., visit 13) * Opioid doses \> 400 mg MME (morphine milligram equivalent) * Women who are pregnant or breastfeeding, or who intend to become pregnant in the 12 weeks from enrollment * Any current unstable or concerning medical condition that would place the patient at increased risk, including hepatic, respiratory, immunological, cardiovascular, endocrine, or renal disease, or in the opinion of the investigator, prevents adherence with the protocol * Need for immediate psychiatric hospitalization * Enrolled in a medical marijuana program * Federal employee
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
4 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Providence VA Medical Center, Providence, RI
RECRUITINGProvidence, Rhode Island, 02908-4734, United States
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South Texas Health Care System, San Antonio, TX
RECRUITINGSan Antonio, Texas, 78229-4404, United States
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VA Connecticut Healthcare System West Haven Campus, West Haven, CT
RECRUITINGWest Haven, Connecticut, 06516-2770, United States
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VA Greater Los Angeles Healthcare System, West Los Angeles, CA
ACTIVE_NOT_RECRUITINGWest Los Angeles, California, 90073-1003, United States
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VA Puget Sound Health Care System Seattle Division, Seattle, WA
TERMINATEDSeattle, Washington, 98108-1532, United States
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VA San Diego Healthcare System, San Diego, CA
RECRUITINGSan Diego, California, 92161-0002, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Zapping nerves without a scalpel: can radiofrequency quiet chronic pain?
- Scientists map the daily rhythms of chronic pain
- Can zapping two brain regions at once quiet chronic nerve pain?
- Can a mindfulness app ease the stress of hospitalization?
- Zapping the brain to loosen stiff legs and quiet nerve pain in MS?
- Ancient Mind-Body practice put to the test for spinal cord injury pain