Clinical Trials Directory

Trials / Completed

CompletedNCT00640432

Safety And Efficacy Of Celecoxib Versus Sodium Diclofenac In The Treatment Of Acute Low Back Pain

A Multicenter, Randomized, Double-Blind, Double-Dummy Study Of The Safety, Tolerability And Efficacy Of Celecoxib 200 Mg Twice A Day (With A 400 Mg Attack Dose) Versus Sodium Diclofenac 75 Mg Twice A Day In Subjects With Acute Low Back Pain

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
244 (actual)
Sponsor
Pfizer's Upjohn has merged with Mylan to form Viatris Inc. · Industry
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

To evaluate the safety and efficacy of celecoxib versus sodium diclofenac in subjects with acute low back pain

Conditions

Interventions

TypeNameDescription
DRUGDiclofenac75 mg oral capsule twice daily for 7 days
DRUGCelecoxib400 mg oral capsule followed by 200 mg oral capsule with the evening meal (\>=4 hours from first dose) on Day 1 then 200 mg oral capsule twice daily for 6 days

Timeline

Start date
2003-10-01
Completion
2004-10-01
First posted
2008-03-21
Last updated
2021-02-02

Locations

9 sites across 1 country: Brazil

Source: ClinicalTrials.gov record NCT00640432. Inclusion in this directory is not an endorsement.