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Search / Trial NCT04088929

The Use of a Water Soluble Under the Tongue (Sublingual) CBD Tablet for Treating Pain Associated With Diabetic Peripheral Neuropathy

Launched by PURE GREEN · Sep 11, 2019

Trial Information

Current as of April 25, 2025

Completed

Keywords

Pain Neuropathy Neuropathic Pain Diabetes

ClinConnect Summary

No description provided

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • 1. Subject is at least 21 years of age;
  • 2. Subject has a diagnosis of chronic diabetic neuropathic pain condition as determined by the subject's health care or allied health provider for which medications other than cannabis, cannabinoids, or cannabis-based medicines are currently utilized;
  • 3. Subject has a 7-day average pain scale score (recorded during the screening period) of ≥ 5;
  • 4. If female, subject is postmenopausal (\> 1 year), surgically sterile, or practicing an approved method of birth control throughout the study and for 5 months (150 days) after the last dose of study drug;
  • 5. If female and of childbearing potential, subject has a denied pregnancy and has no desire to become pregnant throughout the duration of the study;
  • 6. Subject is willing and able to provide his/her written informed consent to participate in the study as stated in the informed consent document;
  • 7. Subject has access to a smart phone and knows how to use smart phone applications.
  • Exclusion Criteria:
  • 1. Subject is pregnant or lactating;
  • 2. Subject has an allergy to cannabis, the Cannabaceae plant family (e.g., hemp, hops, hackberry), PEA, terpenes, peppermint;
  • 3. Subject has a known allergy to active or inert ingredients of Pure Green tablets;
  • 4. Subject is currently treating their pain with cannabis, cannabinoids, cannabis-base medicine;
  • 5. Subject is taking a concomitant medication or treatment that would complicate use or interpretation of the study drug's effects (examples include: Cannabis or any cannabinoid products; Any drug or herbal product that influences the endocannabinoid system (ECS));
  • 6. Subject is taking marijuana (cannabis) in any form, chemicals or extracts or foods or beverages or topical creams, lotions, gels, patches containing marijuana (cannabinoids, or and cannabis derivatives) including synthetic marijuana and/or CBD for at least 30 days prior to this study., and does not promise to not take marijuana (cannabis) in any form, chemicals or extracts or foods or beverages or topical creams, lotions, gels, patches containing marijuana (cannabinoids, or and cannabis derivatives) including synthetic marijuana and/or CBD while participating in this study;
  • 7. Subject is currently being treated with antibiotics for sinus, throat, or lung infections;
  • 8. Subject has shortness of breath associated with allergies;
  • 9. Subject has uncontrolled asthma;
  • 10. Subject has a fever and/or productive cough;
  • 11. Subject does not have access to a smart phone or does not know how to use a smart phone application.

Trial Officials

Debra Kimless, M.D.

Principal Investigator

Pure Green, LLC

About Pure Green

Pure Green is a forward-thinking clinical trial sponsor dedicated to advancing healthcare through innovative research and development. With a focus on sustainable practices and cutting-edge methodologies, Pure Green specializes in conducting high-quality clinical trials across diverse therapeutic areas. The organization is committed to fostering collaboration among stakeholders, ensuring patient safety, and adhering to regulatory standards. By leveraging advanced technologies and a patient-centric approach, Pure Green aims to accelerate the delivery of effective treatments to market, ultimately enhancing the well-being of communities worldwide.

Locations

Sterling Heights, Michigan, United States

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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