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Active Not RecruitingNCT06513507

A Clinical Study to Assess the Efficacy of Cannabigerol in Patients with Active Rheumatoid Arthritis.

Status
Active Not Recruiting
Phase
N/A
Study type
Interventional
Enrollment
12 (actual)
Sponsor
Raphael Pharma · Industry
Sex
All
Age
25 Years
Healthy volunteers
Not accepted

Summary

This is a single-group exploratory longitudinal prospective study lasting 8 weeks. The study aims to measure the efficacy of purified cannabigerol (CBG) in patients with active rheumatoid arthritis using laboratory and self-reported outcome measures.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTCannabigerol (CBG)The daily dose will consist of 50 mg of CBG. Blood tests will be conducted at Baseline, Week 2, Week 4, Week 6, and Week 8 to monitor inflammatory markers and immune response. Self-reported questionnaires will be completed at Baseline, Week 4, and Week 8 to assess symptoms and quality of life.

Timeline

Start date
2024-06-03
Primary completion
2024-12-31
Completion
2024-12-31
First posted
2024-07-22
Last updated
2024-11-21

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT06513507. Inclusion in this directory is not an endorsement.

A Clinical Study to Assess the Efficacy of Cannabigerol in Patients with Active Rheumatoid Arthritis. (NCT06513507) · Clinical Trials Directory