Esophageal Diseases Clinical Trial
Official title:
Investigation of Cannabinoid Receptor Agonist Dronabinol in Patients With Functional Chest Pain
In a recent study, Dronabinol was shown to reduce symptoms in patients with Functional Chest Pain (non-cardiac chest pain). Additionally, metabolic measures and patients' weights were not adversely affected by this regiment. In fact, some cholesterol measures trended in a favorable direction with Dronabinol. The study lasted 28 days and patients took Dronabinol twice daily. The goal of this current study focuses on reducing the dose of Dronabinol to see if the same goals can be achieved. More so, the study will be extended to 12 weeks to gain a more longitudinal picture of therapy with Dronabinol. It is hypothesized that reducing the dose and extending the duration will continue to show an improvement in symptoms as well as no adverse metabolic outcomes.
About 200,000 new cases of Functional Chest Pain (FCP) are diagnosed annually in USA. FCP is
associated with poor quality of life and high health care expenditure. Gastroesophageal
reflux disease (GERD), esophageal motility disorders, and psychological disorders may cause
FCP. However, the mechanism(s) for FCP continue to be explored and include central and
peripheral hypersensitivity as well as biomechanical dysfunction of the esophageal wall. CB1
receptor activation in synaptic clefts fine tunes neuronal firing and may in fact quell the
over excitation associated with hypersensitivity.
Dronabinol, a cannabinoid receptor agonist with a preference for CB1 over CB2, is believed to
reduce the esophageal hypersensitivity. CB1 receptors are located primarily on central and
peripheral neurons (including the enteric nervous system) and myenteric plexus where they
modulate neurotransmitter release. Activation of pre-junctional CB1 receptors may reduce
excitatory enteric transmission and conceivably improve esophageal hyperreactivity and
hypersensitivity, the hallmarks of FCP.
Previously, it was shown that Chest Pain Symptoms were greatly reduced when patients took 5
mg Dronabinol twice daily. Patients had very few side effects from this regiment although
sedation was reported. The goal of this study focuses on reducing the dose of Dronabinol to 5
mg every other day, or essentially, one quarter of the dose. The effect of Dronabinol varies
with CB1 receptor density in various tissues. It is hypothesized that at this reduced dose
relief of chest pain will still be achieved without the sedating effects.
More so, Dronabinol at 5 mg twice daily failed to produce any adverse metabolic outcomes
including measures of glucose, LDL, triglycerides, leptin, or transaminases. Dronabinol
treatment tended to improve some of these measures although the study only lasted 28 days.
Currently the hypothesis is that lower doses at a protracted time course will again fail to
perturb homeostasis.
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