Natural Matrix Protein™ (NMP™) Fibers in Cervical and Lumbar Interbody Fusion

Enrolling by invitation

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

In brief

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.

Key facts

Study ID

NCT06000319

Run by

Induce Biologics USA Inc.

People needed

200

Starts

2024-01-04

Expected to finish

2027-08-01

Last updated by the study team

2025-11-18

Who can join

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

You may qualify if…

• Subject was diagnosed with DDD, spinal stenosis, or spondylolisthesis;
• Subject has undergone cervical or lumbar interbody spine fusion at no more than 3 adjacent levels between C2 and T1 or between L1 and S1;
• Subject has undergone cervical or lumbar interbody spine fusion using NMP Fibers;
• Subject must be 18 years of age or older at the time of consent;
• Subject must be willing and able to sign an informed consent document;
• Subject must be willing and able to return to the study clinic for all follow-up visits, agree to participate in post-operative clinical and radiographic evaluations.

You may not qualify if…

• Subject is under 18 years of age at the time of consent;
• Subject is currently experiencing major mental illness (psychosis, schizophrenia, major affective disorder) which in the opinion of the investigator may indicate that the symptoms are psychological rather than of physical origin;
• Subject is currently imprisoned.

Where it is running

• Alabama Back Institute — Jasper, Alabama, United States

Full record on ClinicalTrials.gov

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