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NCT02814825

An ACDF Multi-Center Study Using ViviGen Cellular Bone Matrix

Completed Last updated 17 February 2026
What this trial tests

trial testing ViviGen in Cervical Spondylosis in 100 participants. Completed in 15 April 2021.

Timeline
1 June 2016
Primary endpoint
22 February 2021
15 April 2021

Quick facts

Lead sponsorDePuy Spine
StatusCompleted
Study typeOBSERVATIONAL
Enrollment100
Start date1 June 2016
Primary completion22 February 2021
Estimated completion15 April 2021

Drugs / interventions tested

Conditions studied

Sponsor

DePuy Spine — full company profile →

Who can join

Adults 21 to 75, any sex, with Cervical Spondylosis or Degenerative Intervertebral Discs. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this post-market study is to collect data on ViviGen and how its use affects fusion rates in the cervical spine when used as additional grafting material to fill the cervical spacer. The patient population of interest is patients who have already elected to undergo a 2-3 level ACDF surgical procedure using ViviGen, per standard of care.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Allografts and Spinal Fusion.
    Cohen JD, Kanim LE, Tronits AJ, Bae HW. · · 2021 · cited 14× · PMID 34376497 · DOI 10.14444/8056

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Other trials of ViviGen

Trials testing the same drug.

Other recruiting trials for Cervical Spondylosis

Currently open trials in the same condition.

Other DePuy Spine trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT02814825.

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