Can Cannabis Help Breathe Easier? New Hope for COPD Patients

Reducing severe breathlessness with dronabinol in the group of patients with severe and very severe chronic obstructive pulmonary disease (BONG): a randomised, double-blinded, placebo-controlled, crossover study in an outpatient clinic in Denmark - a study protocol.

BMJ open • • Moderately Relevant
🤖

AI Summary

Researchers in Denmark are launching an innovative clinical trial to explore the potential of dronabinol, a synthetic form of Δ9-THC, in helping patients with severe chronic obstructive pulmonary disease (COPD) manage their breathlessness. This will be the largest randomized, double-blinded crossover study investigating cannabinoid treatment for COPD patients, offering hope for those struggling with persistent respiratory challenges.

The study will involve 30 patients with severe COPD, who will undergo a carefully designed research protocol. Participants will receive either dronabinol or a placebo for 4 weeks, followed by a 2-week washout period, and then switch to the alternative treatment. Comprehensive monitoring will include lung function tests, quality of life assessments, and continuous tracking of vital signs using a smartwatch, providing a holistic view of the potential therapeutic effects.

By investigating the impact of Δ9-THC on breathlessness, this research aims to provide new insights into alternative treatment options for COPD patients. The study's rigorous design, including approval from medical ethics committees and adherence to international clinical trial guidelines, underscores the scientific approach to exploring cannabinoid-based medical interventions for respiratory conditions.

📄 Original Abstract

Cannabis-based medicine may alleviate breathlessness. This study will investigate whether dronabinol, a synthetic form of Δ9-tetrahydrocannabinol (Δ9-THC), reduces breathlessness in patients with severe and very severe chronic obstructive pulmonary disease (sCOPD) compared to placebo. This single-centre, randomised, double-blinded, placebo-controlled, crossover trial will enrol 30 patients with sCOPD and persistent breathlessness despite optimal treatment. Patients will be recruited from a pulmonary outpatient clinic in Denmark over 24 months. Eligible patients (aged ≥18 years) will receive either dronabinol or placebo for 4 weeks, followed by a 2-week washout, before crossing over to the other treatment for 4 weeks. Exclusion criteria include ongoing infection, substance abuse and significant comorbidities. Primary outcome is breathing discomfort or unpleasantness measured using the 0-10 Numerical Rating Scale. Secondary outcomes include lung function (forced expiratory volume in one second), hair cortisol concentrations, functional tests, plasma THC blood concentrations and questionnaires assessing breathlessness, activity, quality of life, anxiety and depression. Continuous monitoring of vital signs, activity and sleep will be performed using a Garmin Venu 3 smartwatch. Data will be entered into electronic case report forms and monitored by the Good Clinical Practice (GCP) unit in Odense. This will be the largest randomised, double-blinded, crossover trial to investigate dronabinol in patients with COPD and will provide new knowledge on the efficacy and safety. Written informed consents will be obtained from study patients. The study has been approved by the Danish Medicines Agency (case number: 2023010659) and the medical research ethics committees (case number: 2301456). It is registered in the European Union Clinical Trials Registry (2024-513593-22-00) and ClinicalTrials.gov (NCT06473701). The trial follows the Declaration of Helsinki II and International Council for Harmonisation-GCP guidelines. Findings will be disseminated in peer-reviewed publications. The European Union Clinical Trials Registry (2024-513593-22-00) and ClinicalTrials.gov (NCT06473701).

Explore More Research

Stay informed about the latest cannabis science.

Your stash, decoded.