Skip to content

Investigation of Cannabidiol for Reduction of NeuroInflammation in Chronic Back Pain

TerminatedPhase 4NCT03891264
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

In this research, the study team will use brain imaging to evaluate the presence of neuroinflammation in the brains and spinal cords of patients with low back pain, and whether CBD effects levels of neuroinflammation. The efficacy of CBD use for low back pain treatment will also be evaluated by observing whether CBD administration will reduce neuroinflammation and low back pain symptoms.

Study details

Official title
Investigation of Cannabidiol for Reduction of NeuroInflammation in Chronic Back Pain
Conditions
Interventions
Sponsor
Massachusetts General Hospital
Start date
2019-11-13
Primary completion
2020-11-23
Sex
All
Age range
from 18 Years to 75 Years
Results posted
Yes, on ClinicalTrials.gov
Countries
United States
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * age ≥ 18 and ≤ 75; * the ability to give written, informed consent; * ongoing pain that averaged at least 4, on a 0-10 scale of pain during a typical week, and present for at least 50% of days during a typical week; * fluency in English; * on a stable pain treatment (pharmacological or otherwise) for the previous four weeks. * Medical records confirming diagnosis of low back pain * Chronic low back pain, ongoing for at least 6 months prior to enrollment. Exclusion Criteria: * outpatient surgery within 2 months and inpatient surgery within 6 months from the time of scanning; * elevated baseline transaminase (ALT and AST) levels above 3 times the Upper Limit of Normal (ULN), accompanied by elevations in bilirubin above 2 times the ULN * any interventional pain procedures within 6 weeks prior to scanning procedure or at any point during study enrollment; * surgical intervention or introduction/change in opioid regimen at any point during study enrollment * contraindications to functional magnetic resonance imaging scanning and positron emission tomography scanning (including presence of a cardiac pacemaker or pacemaker wires, metallic particles in the body, vascular clips in the head or previous neurosurgery, prosthetic heart valves, claustrophobia); * current or past history within the last 5 years of major medical illness not affecting the central nervous system, other than chronic pain; * implanted spinal cord stimulator (SCS) for pain treatment; * any history of neurological illness or major medical illness affecting the central nervous system, unless clearly resolved without long-term consequences; * current or past history of major psychiatric illness; * PTSD, depression, and anxiety are exclusion criteria only if the conditions were so severe as to require hospitalization in the past year. * pregnancy or breast feeding; * history of head trauma requiring hospitalization; * major cardiac event within the past 10 years; * any use of recreational drugs in the past 3 months * any marijuana use, medical or recreational, in the past 3 months * an abnormal physical exam (e.g., peripheral edema); * routine use of opioids ≥ 60 mg morphine equivalents; * use of immunosuppressive medications, such as prednisone, TNF medications within 2 weeks of the visit; * current bacterial or viral infection; * Any other contraindications to CBD administration noted by the study physician. * If undergoing blood draws through an arterial line during scan, …

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT03891264