Ondansetron 8mg
DrugOndansetron 8 MG prepared in a 100 mL normal saline min-bag
Other names: Zofran
NCT Number: NCT03056482
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
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Notify Me18 year–100 year
All sexes
Interventional
Phase 4
Hotel Dieu Hospital, Kingston, Ontario, Canada
This is a double-blinded, randomized, cross-over clinical trial that will enroll approximately 80 subjects from at least four different research sites. Patients who have been diagnosed with CHS and enrolled in our study will act as their own controls upon their return to the ED for a subsequent bout of CHS for up to 3 visits per subject. Each patient will be allocated in a 1:1:1 fashion into one of three treatment groups: high- or low-dose haloperidol, or ondansetron, with a minimum 7-day washout period between treatments. As CHS tends to be a recurrent syndrome (presumably given the continued use of cannabis despite recommendations to taper and abstain), it is expected that most subjects will return at least once again, and a substantial subset of the study population will complete all three treatment visits during the trial.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Ondansetron 8 MG prepared in a 100 mL normal saline min-bag
Other names: Zofran
Haloperidol 0.05 mg/kg prepared in a 100 mL normal saline min-bag
Other names: Haldol
Haloperidol 0.1 mg/kg prepared in a 100 mL normal saline min-bag
Other names: Haldol
Time frame: 2 hours
Difference between arithmetic mean of Pain Score and Nausea Score (each on a 10-cm VAS) at 2 hours versus at baseline
Time frame: 1, 2, 24 and 48 hours
Changes in abdominal pain score at 1, 2, 24 and 48 hours vs. baseline
Time frame: 1, 2, 24 and 48 hours
Changes in nausea score at 1, 2, 24 and 48 hours vs. baseline
Time frame: 2, 24 and 48 hours
Treatment success = both abdominal pain and nausea score < 2 at 2, 24 and 48 hours
Time frame: 2 hours
Cumulative oral intake from t=0 to 2 hours (in mL)
Time frame: 2 hours
Cumulative emesis from t=0 to 2 hours (in mL)
Time frame: 2 hours
Cumulative urine output (in mL)
Time frame: 2 hours
Deemed discharge-ready at 2 hours in the opinion of the treating physician
Time frame: at discharge from Emergency Department or 12 hours whichever comes first
Given rescue anti-emetics prior to discharge
Time frame: at discharge from Emergency Department or 12 hours whichever comes first
Time interval to discharge-ready from t=0 (min)
Time frame: 2 hours
Subject preference of high- vs low-dose haloperidol, and of haloperidol vs ondansetron (-10, 10)
Time frame: 7 days
Unscheduled return visits to ED within 7 days (count)
Time frame: From time of study intervention until admitting service consulted or subject discharged from Emergency Department, whichever comes first, assessed up to 48 hours
Consulted to admitting service
Time frame: at discharge from Emergency Department or 12 hours whichever comes first
Outcome 10 "Time to Discharge from ED" > 12 hours (binary yes/no)
Dr. Marco L.A. Sivilotti
Other
Haloperidol Versus Ondansetron for Cannabis Hyperemesis Syndrome (HaVOC): A Randomized Controlled Trial
Acronym: HaVOC
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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