drugset / Trial / NCT00894790

Celecoxib Efficacy And Safety Versus Diclofenac In Acute Pain Due To Cervical Sprain Related To A Traffic Accident

NCT00894790

Phase 4 Terminated 8 enrolled Viatris Inc.
RandomizedParallel-groupOpen-labelTreatment

Summary

This Study Will Evaluate Celecoxib Efficacy And Safety Versus Standard Doses Of Diclofenac In Acute Pain Due To Cervical Injury (Due To A Sprain) Related To A Motor Vehicle Accident

Timeline

Start
2009-11
Primary completion
2010-01
Completion
2010-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Celecoxib Other / unclassified 200 mg
Comparator Diclofenac Other / unclassified 75 mg Oral

Indications

No indication recorded.