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NCT Number: NCT07726069

Haloperidol For Outpatient Symptom Management in Patients Diagnosed With Cannabinoid Hyperemesis Syndrome in the Emergrency Department

Patients diagnosed with cannabinoid hyperemesis syndrome that are safe for discharge from the emergency department will be sent an outpatient prescription for haloperidol to be used as needed at home. The study goal is to see if having this medication available helps to prevent return emergency department visits for recurrent or persistent symptoms.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Early Phase 1

Primary location

University of Illinois Hospital

Chicago, Illinois, 60612, United States

Location contact

Drew Posen, PharmD

SUB_INVESTIGATOR

Mason A Bartman, MD

CONTACT

[email protected]

8178972205

Mason A Bartman, MD

PRINCIPAL_INVESTIGATOR

Shaveta Khosla, Khosla

SUB_INVESTIGATOR

Urvi Dubey, BS

SUB_INVESTIGATOR

Wesley Eilbert, MD

CONTACT

[email protected]

6302944225

Wesley Eilbert, MD

PRINCIPAL_INVESTIGATOR

About this study

Cannabinoid hyperemesis syndrome is a relatively new syndrome characterized by nausea, vomiting, and abdominal pain in the setting of excessive cannabis use. This clinical entity has become increasingly prevalent as the concentration of THC has increased in marijuana products over the past several decades. The symptoms have been treated successfully with several medications however the most efficacious appears to be dopamine antagonists such as haloperidol and droperidol. These dopamine antagonists have been used safely and successfully in the inpatient and emergency department settings to decrease the frequency and intensity of nausea, vomiting, and abdominal pain in patients suffering from cannabinoid hyperemesis syndrome. We plan to evaluate haloperidol, a dopamine antagonist available as an oral formulation, as an option for outpatient management of these symptoms.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Patients who meet ROME-4 diagnostic criteria for cannabinoid hyperemesis syndrome

Exclusion criteria

Already on dopamine agonist/antagonist therapy for another condition Parkinson's disease Lewy body dementia Men with QTc > 450 Women with QTc > 460 Patients with documented allergy to haloperidol Patients with known functional prolactinomas Patients who are breastfeeding Patients under the age of 18 Patients who are pregnant Patients who are in the prison system Patients who are unable to consent

Treatment and study plan

Haloperidol

Drug

This intervention involves providing patients an outpatient prescription for as needed haloperidol to attempt to control symptoms of cannabinoid hyperemesis and to attempt to prevent return to the emergency department for that reason.

Primary outcomes

  1. Rate of return to the emergency department

    Time frame: 1 month

    We plan to measure the percentage of people who return to the emergency department for recurrence of symptoms attributable to cannabinoid hyperemesis syndrome

Secondary outcomes

  1. Improvement in symptoms

    Time frame: 1 month

    We plan to report patient reported improvement in symptoms attributable to cannabinoid hyperemesis syndrome

  2. Medication side effects

    Time frame: 1 month

    We plan to report the rate of patient reported side effects that are considered attributable to cannabinoid hyperemesis syndrome

Study contacts

Contact information is provided by the study sponsor or research team.

Mason A Bartman, MD

CONTACT

[email protected]

8178972205

Wesley Eilbert, MD

CONTACT

[email protected]

6302944225

Sponsors and collaborators

Lead sponsor

University of Illinois at Chicago

Other

Registry information

Important dates

Study start
2026
Primary completion
2028
Study completion
2028
First posted
Jul 24, 2026
Registry last updated
Jul 24, 2026

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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