Topical Medication Study for Patients Experiencing Post-Surgical Neuropathic Pain (PNSP)

Study Overview

The primary objective of this study is to demonstrate the effectiveness of a topical medication system in patients with post-surgical neuropathic pain (PNSP).

Are you eligible to participate in this study?

You may be eligible for this study if you meet the following criteria:

Conditions:

• Documented diagnosis of probable or definate PSNP
• Surgery leading to PSNP that was performed at least 6 months to maximally 36 months prior to screening, with PSNP present for at least 6 months prior to screening
• Subject experiencing pain is not currently receiving treatment for PSNP or receives a stable systemic treatment for PSNP that started more than 30 days prior to randomization visit

Age:

• 18 years or older

Gender:

• Female or Male

CONTACT THE RESEARCH TEAM TO LEARN MORE ABOUT THIS STUDY