← Eichor
Study identifier: NCT04775537 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

OssiMend BA in Posterolateral Instrumented Lumbar Fusion

Condition: Spinal Disease · Degenerative Disc Disease  ·  Sponsor: Collagen Matrix

PhaseN/A
Planned participants120
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The primary objective of this study is to measure the success rate of lumbar fusion in subjects at 12 months when instrumented lumbar arthrodesis is performed using OssiMend Bioactive Moldable as the bone grafting material

This description comes directly from the study's public registry record.

Talk to the study team

Meenakshi Paliwal  ·  12014051477  ·  mpaliwal@collagenmatrix.com

Peggy Hansen  ·  201-405-1477  ·  phansen@collagenmatrix.com

Always discuss trial participation with your own doctor first.

Locations (4)

San Diego NeurosurgeryEncinitas, California, United StatesNot Yet Recruiting
Hartford HospitalHartford, Connecticut, United StatesRecruiting
University Orthopaedic Associates, Division of OrthoNJSomerset, New Jersey, United StatesNot Yet Recruiting
McKenzie-willamette Medical CenterEugene, Oregon, United StatesCompleted

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT04775537