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ViviGen Cellular Bone Matrix for Hindfoot or Ankle Arthrodesis — ViviGen  

Ankle Arthritis Clinical Trial

Official title:
Clinical and Radiographic Outcomes Using ViviGen® Cellular Bone Matrix for Complex Hindfoot Arthrodesis

Clinical Trial Summary

To evaluate the fusion status of the hindfoot bones after receiving the ViviGen graft, an FDA approved cellular bone matrix. This is used in a population indicated for hindfoot arthrodesis as an alternative to an autograft.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04138017
Study type Interventional
Source University of Virginia
Contact
Status Enrolling by invitation
Phase Phase 4
Start date October 23, 2018
Completion date January 2024
View Details
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