New protein implant could improve spinal fusion outcomes
NCT ID NCT07217964
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looks at a natural protein called Natural Matrix Protein (NMP) used as a bone graft substitute during lumbar spinal fusion surgery. Researchers will review the medical records of about 100 adults who had this surgery to see how well their bones fused and if there were any complications. The goal is to find out if NMP is a safe and effective option for helping bones heal together in the spine.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Natural Matrix Protein (NMP) bioimplant
- What this could lead to
- If successful, NMP could offer a safer or more effective alternative to traditional bone grafts for spinal fusion surgery.
- What could go wrong
- This is a small, non-randomized study with no control group, so results may not be definitive. The intervention is surgical, carrying standard risks like infection or non-union.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 100 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Mar 2025
- Expected to finish
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Sep 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
hospital patients
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patients experiencing symptomatic lumbar degenerative disc disease who failed conservative management at up to four vertebral levels between L1-S1 between February 2024 and December 2024. * Adult patients (≥ 18 years old) who underwent lumbar fusion with an NMP graft and interbody cage Exclusion Criteria: * Previous lumbar fusion attempts at the level of surgery (adjacent lumbar levels are acceptable) * Active Malignancy * Concurrently under chemotherapy * Active infection at time of surgery * Mentally compromised * Trauma to the operated region
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Hospital for Special Surgery
New York, New York, 10021, United States
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