TerminatedPhase 4

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

Stopped: See termination reason in detailed description.

Mexico8 participantsStarted 2009-11

Plain-language 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

Who can participate

Age range18 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Patients That Had Suffered A Car Accident And Due To It Suffered A Cervical Sprain Exclusion Criteria: * Recent Cervical Sprains Or Other Cervical Conditions

What they're measuring

Change From Baseline to Day 7 of Participant's Assessment of Cervical Pain Due to Cervical Sprain

Timeframe: Baseline, Day 7

Trial details

NCT IDNCT00894790

SponsorPfizer's Upjohn has merged with Mylan to form Viatris Inc.

Sponsor typeINDUSTRY

Study typeINTERVENTIONAL

Primary completion2010-01

Results submitted2011-01-28

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