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

Viatris

Status and phase: Terminated; Phase 4

Conditions: Pain

Treatments: Drug: oral Diclofenac; Drug: Celecoxib

Study type: Interventional

Funder types: Industry

Identifiers

NCT00894790

A3191352

Details and patient eligibility

About

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

Full description

On 21Oct2010 study was prematurely terminated due to poor enrollment with subsequent low number of participants. No safety or efficacy issues were involved in the decision to terminate prematurely.

Enrollment: 8 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

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

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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8 participants in 2 patient groups

1

Experimental group

Treatment:

Drug: Celecoxib

2

Active Comparator group

Treatment:

Drug: oral Diclofenac