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BD Completes Enrollment in PREVENT Trial of Phasix Mesh for Hernia Prevention

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BD has completed enrollment in the PREVENT clinical trial evaluating Phasix™ Mesh to prevent incisional hernias after abdominal surgery, addressing a significant unmet need. The randomized study enrolled 477 patients across 32 sites in the United States and Europe, using a resorbable prophylactic mesh. Patients will be followed for a primary endpoint at 24 months, with longer-term follow-up planned through five years.

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