Fibergraft Interbody Fusion Retrospective

Completed

Conditions studied: Degenerative Disc Disease, Degenerative Spondylolisthesis, Spinal Degeneration, Spinal Stenosis

In brief

A single center study of clinical and radiological outcomes in a retrospective cohort of patients treated with Lumbar Interbody Fusion augmented with Prosidyan Fibergraft for 1 or 2 level degenerative spinal disease by a single surgeon. Study Design: Retrospective chart review with prospective data collection.

Key facts

Study ID

NCT03898232

Run by

Bone and Joint Clinic of Baton Rouge

People needed

66

Starts

2019-05-09

Expected to finish

2020-02-20

Last updated by the study team

2021-01-29

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• - Previous Lumbar Interbody Fusion (LIF) at 1-3 levels augmented with Prosidyan Fibergraft Putty.
• No revision or device removal at the operative level(s).
• Patient did not undergo a Lumbar CT at least 8 months post-operatively.
• Willing and able to sign Informed Consent.
• Willing and able to complete questionnaires and undergo CT scan of the Lumbar Spine

Where it is running

• Bone and Joint Clinic of Baton Rouge — Baton Rouge, Louisiana, United States

Full record on ClinicalTrials.gov

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