Geneva, Aug. 6 -- International Clinical Trials Registry received information related to the study (NCT07726069) titled 'Haloperidol For Outpatient Symptom Management in Patients Diagnosed With Cannabinoid Hyperemesis Syndrome in the Emergrency Department' on July 21.
Study Type: Interventional
Study Design:
Allocation: N/A. Intervention model: Single Group Assignment. Primary purpose: Treatment. Masking: None (Open Label).
Primary Sponsor: University of Illinois at Chicago
Condition:
Cannabinoid Hyperemesis Syndrome
Intervention:
Drug: Haloperidol
Recruitment Status: Not recruiting
Phase: Early Phase 1
Date of First Enrollment: November 2026
Target Sample Size: 100
Countries of Recruitment:
United States
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