Haloperidol Versus Ondansetron for Cannabis Hyperemesis Syndrome (HaVOC) (NCT03056482) | Clinical Trial Compass
CompletedPhase 4
Haloperidol Versus Ondansetron for Cannabis Hyperemesis Syndrome (HaVOC)
Canada33 participantsStarted 2017-05-21
Plain-language summary
Cannabis Hyperemesis Syndrome (CHS) has become a well-documented syndrome since 2004 and is expected to increase in prevalence with continuing liberalization of marijuana and recognition of the disease. Regardless of whether the association with heavy cannabis use is recognized, there is well-documented resistance to traditional anti-emetic treatment. Given promising reports of the use of intravenous haloperidol, a randomized controlled trial comparing it to the commonly administered anti-emetic ondansetron will contribute to the management of CHS
Who can participate
Age range18 Years – 100 Years
SexALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion criteria
✓. Age \> 18 years
✓. Self-report of ≥3 episodes of emesis occurring in a cyclic pattern for greater than 1 month in the preceding 2 years
✓. Current episode \>2 hours of emesis
✓. At least one episode of emesis/forceful retching witnessed (including products of emesis at bedside) or heard by an independent observer (healthcare provider or family/friend) in the emergency department
✓. Self-reported frequent (near daily to daily x at least 6 months) use of cannabis by inhalation.
✓. Working diagnosis of cannabis hyperemesis syndrome in the opinion of the treating emergency physician
Exclusion criteria
✕. Chronic, daily use of opioid equivalent to ≥10mg morphine/day
✕. Inability to comprehend study consent or instructions
✕. Unreliable follow-up/unlikely to return for cross-over
✕. Administration of an intravenous antiemetic, anticholinergic or antipsychotic (other than up to 100mg dimenhydrinate) in the previous 24 hours
✕. Allergy or intolerance to haloperidol or ondansetron
✕. Pregnancy
✕. Any other medical or psychiatric condition that in the opinion of the enrolling physician would interfere with participation in the trial