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Topical Medication Study for Patients Experiencing Post-Surgical Neuropathic Pain (PNSP)
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:
- 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
- 18 years or older
- Female or Male
CONTACT THE RESEARCH TEAM TO LEARN MORE ABOUT THIS STUDY