Trials / Completed
CompletedNCT04764344
Haloperidol for the Treatment of Nausea and Vomiting in the ED
A Single Center, Randomized Controlled Prospective Double-blinded Trial Comparing Haloperidol to Standard Ondansetron Therapy for Control of Nausea and Vomiting in the Emergency Department
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 60 (actual)
- Sponsor
- Western Michigan University School of Medicine · Academic / Other
- Sex
- All
- Age
- 18 Years – 55 Years
- Healthy volunteers
- Not accepted
Summary
Single center, double-blind, randomized, controlled trial in patients who present to the emergency department (ED) with a chief complaint of nausea or vomiting. A total of 300 patients age 18-55 presenting to the emergency department with chief complaint of nausea or vomiting will be enrolled from February 2021 - February 2022. Patients will be randomized and symptom levels will be recorded at 30, 60, 90, minutes. Follow-up will be performed by telephone at 24 hours.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Haloperidol | 2.5mg of IV haloperidol will be diluted to 5ml with 0.9% NS and given over 2 minutes IVP |
| DRUG | Ondansetron | Ondansetron |
Timeline
- Start date
- 2021-04-01
- Primary completion
- 2023-05-22
- Completion
- 2023-05-22
- First posted
- 2021-02-21
- Last updated
- 2023-06-01
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT04764344. Inclusion in this directory is not an endorsement.