Recruitment

Recruitment Status
Not yet recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Abdominal Pain
  • Cannabis Use
  • Nausea
  • Vomiting
Type
Interventional
Phase
Phase 4
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentIntervention Model Description: This is a single-center prospective randomized double-blinded non-inferiority trial with potential assessment of superiority comparing haloperidol to ondansetron for the treatment of nausea and vomiting.Masking: Triple (Participant, Care Provider, Investigator)Masking Description: Treatment allocations will be revealed only after study completion, unless there is concern for a serious adverse event in which case treatment team and patient will be unblinded. Interim analysis will be performed at 150 participants to evaluate for effectiveness and powerPrimary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 55 years
Gender
Both males and females

Description

Not Provided

Not Provided

Tracking Information

NCT #
NCT04764344
Collaborators
Not Provided
Investigators
Principal Investigator: Jessica McCoy, MD Western Michigan University School of Medicine