The Safety, Tolerability and Efficacy of Dronabinol, for the Treatment of Nausea and Vomiting in β¦ (NCT02608931) | Clinical Trial Compass
WithdrawnPhase 2
The Safety, Tolerability and Efficacy of Dronabinol, for the Treatment of Nausea and Vomiting in Familial Dysautonomia
Stopped: Unable to begin study with drug provider
United States0Started 2015-11
Plain-language summary
This is a pilot clinical trial of dronabinol to treat disabling attacks of nausea and vomiting in patients with familial dysautonomia (FD, also known as Riley Day syndrome or hereditary sensory and autonomic neuropathy type III). FD is a rare autosomal recessive disease in which the growth and development of selective nerves is impaired. Patients with FD suffer recurrent uncontrollable nausea and vomiting crises accompanied by skin flushing, tachycardia and arterial hypertension. Current treatments of nausea are ineffective or have intolerable side sides. Our long-term goal is to treat nausea effectively and without side effects, a therapeutic intervention that would markedly improve the quality of life of patients with FD.
Who can participate
Age range18 Years β 60 Years
SexALL
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Inclusion criteria
β. Male or female patients aged 18-60.
β. Confirmed diagnosis of familial dysautonomia by genetic testing.
β. Symptoms of severe nausea.
β. Able to swallow the capsules.
β. Written informed consent or ascent to participate in the pilot trial and understanding that they can withdraw consent or accent at anytime without affecting their future care.
β. Ability to comply with the requirements of the study procedures, including taking blood pressure measurements at home
Exclusion criteria
β. Patients with a history of hypersensitivity to any cannabinoid or sesame oil.
β. Cannabinoid use in the previous 4 weeks (a urinary cannabinoid test will be performed before study entry).
β. Patients with a history of substance abuse, including alcohol abuse or dependence, or marijuana.