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Upstate Active Clinical Trials

Study Title:

A Multi-center, Prospective, Single Arm Study of Patients Undergoing a
Two or Three Level ACDF Using ViviGen® Cellular Bone Matrix in
Conjunction with Cervical Allograft Spacers and DePuy Synthes Spine
Anterior Cervical Plate Systems

What is the purpose of the study? (in Layman's terms, please describe the study)

This post-market study is being done to collect data on a product called ViviGen®. A post-market study is when data is collected on product(s) that are commercially available and in general use by surgeons so that more ‘real-time’ data becomes available to the scientific community. This study will collect data about how ViviGen will affect fusion rates in the cervical (neck) region of your spine following cervical spine surgery in a procedure called Anterior Cervical Discectomy and Fusion (ACDF).

Upstate Institutional Review Board (IRB) Number:

920313

Study/Protocol ID:

DSS-2015-01

Study Phase:

N/A

Patient Age Group:

Adults

Principal Investigator:

William F Lavelle, MD

Who can I contact for more information?

Name: Tina M Craig
Phone: 315-464-8618
Email: [email protected]

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