102
Participants
Start Date
April 30, 2003
Primary Completion Date
April 30, 2003
Lidoderm®
Eligible patients were randomized equally to one of two groups: lidocaine patch 5% or matching placebo patch. During the 6-week treatment period, patients used up to three patches daily applied q24h.
Lidoderm®
Eligible patients were randomized equally to one of two groups: lidocaine patch 5% or matching placebo patch. During the 6-week treatment period, patients used up to three patches daily applied q24h.
Birmingham
Hueytown
Phoenix
Mill Valley
Allentown
Salt Lake City
Lead Sponsor
Endo Pharmaceuticals
INDUSTRY