drugset / Trial / NCT05248984

Dosing of Ketorolac Impacts Post-cesarean paiN manaGemenet (KING)

NCT05248984

Phase 4 Completed 92 enrolled Ohio State University
RandomizedParallel-groupSingle-blindTreatment

Summary

This is a randomized controlled single blinded trial to compare the morphine milligram equivalents (MME) use in the first 24 hours postoperatively after cesarean section in patients receiving a single dose of 30 mg intravenous ketorolac vs. 60 mg intravenous ketorolac in the operating room after the end of surgery.

Timeline

Start
2022-06-08
Primary completion
2023-11-30
Completion
2023-11-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Ketorolac Other / unclassified 30 mg Intravenous
Subject Ketorolac Other / unclassified 60 mg Intravenous

Indications

No indication recorded.