drugset / Trial / NCT03278691

Ketorolac on Posterior Thoracolumbar Spinal Fusions

NCT03278691

Phase 4 Unknown 600 enrolled Henry Ford Health System
RandomizedParallel-groupQuadruple-blindTreatment

Summary

To determine is low-dose ketorolac use in the early post-operative period (within 48 hours) provides adequate analgesia without long term adverse effect on spinal fusion rates when compared to post-operative analgesia without the use of NSAIDs.

Timeline

Start
2017-10-03
Primary completion
2023-12-31
Completion
2025-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Ketorolac Other / unclassified 15 mg Intravenous

Indications

No indication recorded.