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Completed

NCT Number: NCT03056482

Haloperidol Versus Ondansetron for Cannabis Hyperemesis Syndrome (HaVOC)

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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Key information

Age range

18 year–100 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Hotel Dieu Hospital, Kingston, Ontario, Canada

Loading trial locations.

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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
  • Current active participation in an investigational drug trial

Treatment and study plan

Ondansetron 8mg

Drug

Ondansetron 8 MG prepared in a 100 mL normal saline min-bag

Other names: Zofran

Haloperidol 0.05mg/kg

Drug

Haloperidol 0.05 mg/kg prepared in a 100 mL normal saline min-bag

Other names: Haldol

Haloperidol 0.1mg/kg

Drug

Haloperidol 0.1 mg/kg prepared in a 100 mL normal saline min-bag

Other names: Haldol

Primary outcomes

  1. Change in pain and nausea

    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

Secondary outcomes

  1. Change in pain

    Time frame: 1, 2, 24 and 48 hours

    Changes in abdominal pain score at 1, 2, 24 and 48 hours vs. baseline

  2. Change in nausea

    Time frame: 1, 2, 24 and 48 hours

    Changes in nausea score at 1, 2, 24 and 48 hours vs. baseline

  3. Treatment success

    Time frame: 2, 24 and 48 hours

    Treatment success = both abdominal pain and nausea score < 2 at 2, 24 and 48 hours

  4. Oral intake

    Time frame: 2 hours

    Cumulative oral intake from t=0 to 2 hours (in mL)

  5. Emesis volume

    Time frame: 2 hours

    Cumulative emesis from t=0 to 2 hours (in mL)

  6. Urine output

    Time frame: 2 hours

    Cumulative urine output (in mL)

  7. Discharge ready at 2 hours

    Time frame: 2 hours

    Deemed discharge-ready at 2 hours in the opinion of the treating physician

  8. Rescue anti-emetics in ED

    Time frame: at discharge from Emergency Department or 12 hours whichever comes first

    Given rescue anti-emetics prior to discharge

  9. Time to discharge from ED

    Time frame: at discharge from Emergency Department or 12 hours whichever comes first

    Time interval to discharge-ready from t=0 (min)

  10. Subject preferred arm

    Time frame: 2 hours

    Subject preference of high- vs low-dose haloperidol, and of haloperidol vs ondansetron (-10, 10)

  11. Return to ED

    Time frame: 7 days

    Unscheduled return visits to ED within 7 days (count)

  12. ED consult

    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

  13. Prolonged ED Length of stay

    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)

Sponsors and collaborators

Lead sponsor

Dr. Marco L.A. Sivilotti

Other

Registry information

Official study title

Haloperidol Versus Ondansetron for Cannabis Hyperemesis Syndrome (HaVOC): A Randomized Controlled Trial

Acronym: HaVOC

Important dates

Study start
2017
Primary completion
2019
Study completion
2019
First posted
Feb 17, 2017
Registry last updated
Apr 3, 2024

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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