RecruitingPhase 4NCT05776953
Evaluation of the Effects of Ketorolac Dose on Duration of Analgesia in Emergency Department (ED) Renal Colic Patients
Evaluation of the Effects of Ketorolac 15mg IV Versus 30mg IV on Duration of Analgesia in Patients Who Present to the Emergency Department With Renal Colic
Sponsor
Hackensack Meridian Health
Enrollment
86 participants
Start Date
Dec 21, 2023
Study Type
INTERVENTIONAL
Conditions
Summary
This is a prospective interventional study examining the effect of ketorolac at doses of 15mg versus 30 mg for duration of analgesia in emergency department patients with suspected renal colic.
Eligibility
Min Age: 18 YearsMax Age: 65 Years
Inclusion Criteria5
- Patients will be included if they present to the Emergency Department with (all of the following):
- Adult emergency department patients \< 65 years old
- One or more of the following common ED chief complaints associated with the suspected diagnosis of renal colic. These chief complaints include but are not limited to: flank pain, back pain, abdominal pain, left and/or right lower quadrant pain, and/or pelvic pain
- Pain score of 4 or greater on the 0-10 NRS
- Determination of treatment with IV ketorolac
Exclusion Criteria8
- Patients will be excluded if any of the following apply:
- Allergy to ketorolac
- Pregnant patients
- Previously received analgesic medications within 4 hours prior to administration of ketorolac in our ED
- Known or stated history of renal insufficiency
- Body weight \< 50 kg
- Age greater than 65 years
- Patients that do no read/write Spanish or English
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Interventions
DRUGKetorolac
IV Ketorolac for pain
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT05776953
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