Trials / Terminated
TerminatedNCT00904605
Lidocaine Patch Versus Celecoxib in Pain From Osteoarthritis of the Knee
A Randomized, Open-Label Study Comparing the Efficacy and Safety of Lidocaine Patch 5% With Celecoxib 200 mg in Patients With Pain From Osteoarthritis of the Knee
- Status
- Terminated
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- —
- Sponsor
- Endo Pharmaceuticals · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Patients with unilateral or bilateral osteoarthritis of the knee participated in a Phase IV clinical trial to assess the efficacy of Lidoderm compared with celecoxib 200mg in treating pain from osteoarthritis of the knee.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Lidoderm | Eligible patients were randomly allocated to receive one of two treatments for 12 weeks: lidocaine patch 5% or celecoxib 200 mg daily. Lidocaine patch 5% (Lidoderm®, Endo Pharmaceuticals Inc.), 1⅓ patches applied topically to each affected knee every 24 hours (q24h |
| DRUG | Celecoxib | Eligible patients were randomly allocated to receive one of two treatments for 12 weeks: lidocaine patch 5% or celecoxib 200 mg daily. Lidocaine patch 5% (Lidoderm®, Endo Pharmaceuticals Inc.), 1⅓ patches applied topically to each affected knee every 24 hours (q24h) |
Timeline
- Start date
- 2004-06-01
- Primary completion
- 2004-11-01
- Completion
- 2004-11-01
- First posted
- 2009-05-19
- Last updated
- 2010-02-15
Locations
20 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT00904605. Inclusion in this directory is not an endorsement.