Evaluating the Impact of a Novel Cannabinoid Product for Endometriosis

Recruitment Status
RECRUITING
(See Contacts and Locations)Verified February 2026 by Mclean Hospital
Sponsor
Mclean Hospital
Information Provided by (Responsible Party)
Staci Gruber, Ph.D.
Clinicaltrials.gov Identifier
NCT06477406
Other Study ID Numbers:
2024P001549
First Submitted
June 20, 2024
First Posted
June 26, 2024
Last Update Posted
March 29, 2026
Last Verified
February 2026

ClinicalTrials.gov processed this data on March 2026Link to the current ClinicalTrials.gov record .

History of Changes

Study Details

Study Description

Despite recent increases in both medical and recreational cannabis use in the United States and globally, little research has been conducted to determine the potential applications for womens health. Endometriosis impacts approximately 10% of women of reproductive age, an estimated 176 million individuals, and is characterized by endometrial cells growing outside of the uterus, resulting in severe pain, chronic inflammation, gastrointestinal symptoms, infertility, and often, depression and anxiety (WHO, 2023). Existing treatment options are often limited in efficacy and may result in a variety of negative side effects. Previous research has indicated that cannabinoids including cannabidiol (CBD), delta-9 tetrahydrocannabinol (THC), and a number of other cannabinoids may hold potential for treating the symptoms of endometriosis, especially the chronic pain associated with the condition.

This study is a double-blind crossover clinical trial of a high-CBD product compared to placebo over a total of 12 weeks of treatment in patients with endometriosis. Participants will complete 7 visits over 12 weeks; 4 visits will be conducted in-person at McLean Hospital in Belmont, MA, and 3 visits will be conducted remotely. Visits consist of clinical ratings, assessments of conventional medication use, quality of life measures, and providing saliva, urine, and blood samples.

Condition or DiseaseIntervention/Treatment
Endometriosis
Drug: CannabidiolDrug: Placebo

Study Design

Study TypeInterventional
Actual Enrollment30 participants
Design AllocationNon-Randomized
Interventional ModelCrossover Assignment
MaskingDouble
Primary PurposeTreatment
Official TitleEvaluating the Impact of a Novel Cannabinoid Product for Endometriosis
Study Start DateFebruary 26, 2024
Actual Primary Completion Date2w 4d from now
Actual Study Completion Date2w 4d from now

Groups and Cohorts

Group/CohortIntervention/Treatment
High-CBD Sublingual Product
A custom-formulated, hemp-derived, full-spectrum high-CBD sublingual solution; 0.75mL of solution will be self-administered three times daily (TID) for the duration of the CBD phase.
Drug: Cannabidiol
Custom formulation of a hemp-derived sublingual solution that is high in CBD and includes other cannabinoids and terpenes.
Placebo
Placebo solution (0.75mL) will be self-administered TID for the duration of the placebo phase.
Drug: Placebo
An active placebo containing supplemental terpenes matched to the high-CBD product.

Outcome Measures

Primary Outcome Measures
  1. Visual Analog Scale (VAS)
    The VAS is a commonly used pain scale where patients draw a line to indicate their pain level on a 100 millimeter long line anchored by two verbal descriptors for symptom extremes (e.g. "no pain" to "worst imaginable pain"). The VAS will be used to describe different types of endometriosis-related pain (dysmenorrhea (pain during menstruation), dyspareunia (pain during or after intercourse), and non-menstrual chronic pelvic pain). Lower scores indicate less pain.
Secondary Outcome Measures
  1. Endometriosis Health Profile (EHP-30)
    The EHP-30 is a well-validated self-report scale with 30 core items and 23 additional questions related to specific modules and areas of life often impacted by endometriosis symptoms. Lower scores indicate fewer symptoms.
  2. VAS-IBS
    The VAS-IBS queries bowel-related concerns. While initially developed for IBS patients, it is commonly used to assess gastrointestinal symptoms in endometriosis patients. Lower scores indicate fewer bowel symptoms.
  3. Beck Anxiety Inventory (BAI)
    The BAI is a 21 item-self-report measure that can be used to screen for anxiety. Each item on the BAI is rated on a scale of 0 to 3, and is descriptive of subjective, somatic, or panic-related symptoms of anxiety. Lower scores indicate fewer symptoms of anxiety.
  4. Beck Depression Inventory (BDI)
    The BDI is a 21 item-self-report measure that can be used to assess the severity of depression. Each item on the BDI relates to a symptom of depression and is rated by the subject using a 0-3 scale. Lower scores indicate fewer depressive symptoms.
  5. Conventional Medication Use
    Changes in conventional medication use will be assessed over the course of treatment with study product.
  6. Inflammatory Biomarkers
    Saliva samples will be used to quantify levels of common inflammatory markers (e.g. IL-1β, IL-6, IL-8, TNF-α). Lower levels of inflammatory markers indicate less systemic inflammation.
  7. Circulating Endocannabinoid Concentrations
    Plasma will be analyzed for circulating levels of endocannabinoids and related compounds (e.g., AEA, 2-AG, 2-OG, PEA, OEA).

Eligibility Criteria

Ages Eligible for Study(Adult, Older Adult)
Sexes Eligible for StudyFemale
Accepts Healthy VolunteersNo
Inclusion Criteria
1. Subject has provided informed consent 2. Sex assigned female at birth 3. Subject is 21 or older 4. Subject is fluent in English 5. Subject endorses at least moderate levels of pain at the baseline visit 6. Subject endorses having endometriosis
Exclusion Criteria
1. Non-fluent English speakers 2. Endorsement of current substance use disorder, psychotic disorder, or an eating disorder 3. Currently uses cannabis or cannabinoid products regularly 4. Patients will be excluded if they have a positive urine pregnancy test, are trying to become pregnant, or are currently breastfeeding 5. Presence of a serious or unstable medical illness, including liver, kidney, or cardiovascular disease (hyper/hypotension, cardiac disorders), or neurological disorder (including seizure disorder) 6. Neuropathic pain or cancer-related pain 7. Disclosure of a genetic polymorphism affecting CYP2C9 function

Contacts and Locations

Sponsors and CollaboratorsMclean Hospital
Locations
McLean Hospital | Belmont Massachusetts, United States, 02478
Investigators
Principal Investigator: Staci Gruber, PhD, Mclean Hospital