A Phase 2 randomized study of NEUROCUPLE™ in TKA patients

Completed Not Applicable NCT06460350

Study Description

Evaluating the effectiveness of NEUROCUPLE™ pain relief patch for reducing pain and opioid use after knee replacement surgery

Study Details

Registry ID:
NCT06460350
Conditions:
Total Knee Arthroplasty
Phase:
Not Applicable
Target Enrollment:
156 participants
Start Date:
Age Range:
18–999 years
Healthy Volunteers:
No

Study Locations (1 site)

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