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
| Type | Name | Description |
|---|---|---|
| DRUG | Diclofenac | 75 mg oral capsule twice daily for 7 days |
| DRUG | Celecoxib | 400 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.