Lidoderm® (Lidocaine Patch 5%) in Diabetic and Idiopathic Neuropathy

PHASE4CompletedINTERVENTIONAL
Enrollment

76

Participants

Timeline

Start Date

April 30, 2002

Primary Completion Date

June 30, 2003

Conditions
Diabetes
Interventions
DRUG

Lidoderm

Patients participated in an 8-week treatment period; patients at one site were to continue treatment for the entire 8 weeks while patients at two sites were to terminate treatment after 3 weeks. Commercially available Lidoderm® (lidocaine patch 5%) was provided to each patient with up to four patches applied topically 18 hours on, 6 hours off per day to the area of maximal peripheral neuropathic pain.

Trial Locations (4)

Unknown

Birmingham

Hueytown

Jacksonville

Rochester

Sponsors
All Listed Sponsors
lead

Endo Pharmaceuticals

INDUSTRY