About this trial
This exploratory, proof-of-concept study is a double-blind (participants and investigators will be blinded), placebo-controlled, randomized, two-arm clinical trial of Marinol \[dronabinol, synthetic Δ9-tetrahydrocannabinol (THC)\] for chronic low back pain (cLBP) with a 2:1 allocation ratio. Up to 75 subjects will be enrolled in this pilot study and randomized to receive doses of THC (up to 30 mg/day), orally, over 8 weeks. This study will be conducted at a single site; it does not include any stratifications, and there is no interim analysis planned. Notably, the goal is to determine whether there is enough evidence of the safety of THC to support the development of later-phase clinical trials. Thus, detailed developmental plans are contingent on the outcomes of this study.
Eligibility criteria
Qualifiers
Provision of signed and dated informed consent form.
Stated willingness to comply with all study procedures and availability for the duration of the study.
Ability to take oral medication per protocol.
Male or female, aged 18-64 years.
Disqualifiers
Non-English speaking or inability to read and understand English.
Current and unwilling to stop the use of cannabis/marijuana and any other cannabinoids, including over the counter CBD products.
Reported allergic reactions to cannabis, CBD, THC, or components of the study interventions.
Have Blood Urea Nitrogen or Creatinine levels outside the normal range, or other clinically significant laboratory abnormalities.
Trial design
Treatments tested in this trial
- Dronabinol
- Placebo
Treatment groups
Sponsors and collaborators
Christopher D. Verrico
Lead sponsor
Baylor College of Medicine
Sponsor institution