Evaluation of the Effects of Ketorolac Dose on Duration of Analgesia in Emergency Department (ED) Renal Colic Patients
Renal Colic, Flank Pain, Emergencies
About this trial
This is an interventional treatment trial for Renal Colic
Eligibility Criteria
Inclusion Criteria: Patients will be included if they present to the Emergency Department with (all of the following): Adult emergency department patients < 65 years old Complaint of flank pain Pain score of 4 or greater on the 0-10 NRS Determination of treatment with IV ketorolac Exclusion Criteria: 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 (eGFR < 50 ml/min/1.73 m2) Body weight < 50 kg Age greater than 65 years
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
15mg IV Ketorolac
30mg IV Ketorolac
Patients will be randomized to 15mg IV ketorolac
Patients will be randomized to 30mg IV ketorolac