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NCT06477406Active, not recruitingPhase 2

Evaluating the Impact of a Novel Cannabinoid Product for Endometriosis

Source: ClinicalTrials.gov · Last updated 30 Sept 2026

Brief summary (registry, in English)

Despite the proliferation of cannabis and cannabinoid products in recent years, little research has been done to determine the impact of these products on womens health conditions, including endometriosis. This study is designed to assess the impact of a custom-formulated, hemp-derived, full-spectrum, high-CBD product vs. placebo on clinical symptoms and biomarkers over the course of 12 weeks of treatment in patients with endometriosis. This project will provide information that does not currently exist on the potential efficacy of a cannabinoid-based sublingual product for endometriosis.

Status (registry)
Active, not recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
30 (estimated)
First submitted
21 Jun 2024
Start date
27 Feb 2024
Primary completion date
Dec 2026
Lead sponsor
Mclean Hospital
NCT number
NCT06477406

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 30
  • From 27 Feb 2024 to the primary completion date, Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Endorsement of current substance use disorder, psychotic disorder, or an eating disorder
  • Presence of a serious or unstable medical illness, including liver, kidney, or cardiovascular disease (hyper/hypotension, cardiac disorders), or neurological disorder (including seizure disorder)
  • Neuropathic pain or cancer-related pain

Other

  • Non-fluent English speakers
  • Currently uses cannabis or cannabinoid products regularly
  • Patients will be excluded if they have a positive urine pregnancy test, are trying to become pregnant, or are currently breastfeeding
  • Disclosure of a genetic polymorphism affecting CYP2C9 function

Who the study is looking for

  • Subject has provided informed consent
  • Sex assigned female at birth
  • Subject is 21 or older
  • Subject is fluent in English
  • Subject endorses at least moderate levels of pain at the baseline visit
  • Subject endorses having endometriosis

Age in the registry: 21 years to - · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
McLean Hospital
Coordinator of this site? Confirm its status
BelmontUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.