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NCT03464461 Clinical Trial

Dosing of Ketorolac in the Emergency Department

Acute Pain Clinical Trial

Official title:
Dosing of Ketorolac for Four Classes of Complaints in the Emergency Department

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT03464461
Other study ID # 2010856
Secondary ID
Status Active, not recruiting
Phase Phase 4
First received
Last updated
Start date May 1, 2018
Est. completion date August 1, 2025

Study information
Verified date July 2023
Source University of Missouri-Columbia
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The optimal dose of ketorolac in the Emergency Department setting is no clear. We will compare 3 doses to determine the optimal dose.

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.

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 500
Est. completion date August 1, 2025
Est. primary completion date May 31, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: > 18 y/o Exclusion Criteria: pregnant allergic other contraindication

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• Ketorolac
IV drug

Locations
Country Name City State
United States University of Missouri Health Care Columbia Missouri

Sponsors (1)
Lead Sponsor Collaborator
University of Missouri-Columbia

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Intensity of pain pain score on 0-10 scale 30 minutes
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