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Clinical Trial Summary

The aim of this study is to evaluate the effectiveness and safety of Natural Matrix Protein™ (NMP™) fibers when used in cervical or lumbar interbody fusion in patients with degenerative disc disease (DDD), spinal stenosis, spondylolisthesis undergoing cervical or lumbar interbody spine fusion at no more than 3 adjacent levels.


Clinical Trial Description

The study involves a retrospective review of patients' medical records and prospective collection of X-rays, and patient outcome questionnaires. The study population will include 100 consecutive lumbar interbody fusion and 100 consecutive cervical interbody fusion patients who meet the inclusion criteria and do not meet the exclusion criteria. There will be 4 prospective study visits following consent. Follow-up will occur in accordance with standard of care practice and will continue to 12 months post-surgery ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06000319
Study type Observational
Source Induce Biologics USA Inc.
Contact Sean A Peel, Ph.D.
Phone 416-898-9724
Email sean.peel@redrockregen.com
Status Not yet recruiting
Phase
Start date September 2023
Completion date December 2025

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