Trials / Terminated
TerminatedNCT03464461
Dosing of Ketorolac in the Emergency Department
Dosing of Ketorolac for Four Classes of Complaints in the Emergency Department
- Status
- Terminated
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 289 (actual)
- Sponsor
- University of Missouri-Columbia · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The optimal dose of ketorolac in the Emergency Department setting is no clear. We will compare 3 doses to determine the optimal dose.
Detailed description
Patients from 4 groups will be treated with 3 different doses of ketorolac. The groups are 1. headache 2. abdominal pain 3. musculo-skeletal pain 4. viral syndrome. The doses will be 0, 10, 30mgs of ketorolac to clarify the placebo effect and the optimal dosage as a function of condition.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Ketorolac | IV drug |
Timeline
- Start date
- 2018-05-01
- Primary completion
- 2024-05-30
- Completion
- 2024-05-30
- First posted
- 2018-03-14
- Last updated
- 2024-11-05
- Results posted
- 2024-11-05
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT03464461. Inclusion in this directory is not an endorsement.