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OssiMend BA in Posterolateral Instrumented Lumbar Fusion
RecruitingObservational study
OssiMend Bioactive Moldable in Posterolateral Instrumented Lumbar Fusion
Who can join
Ages 18 and older · All sexes
Full eligibility criteria
Inclusion Criteria: * Subject must be 18 years of age or older at the time of consent and must have a documented diagnosis of degenerative disc disease (DDD) that has failed to respond to nonoperative treatment for at least 6 months. DDD is defined by back and/or radicular pain with degeneration of the disc as confirmed by medical history, physical examination, and radiographic studies that may include CT, MRI, plain X-ray film, discography, myelography, etc. with one or more of the following findings: * Instability as defined by \>3mm translation or \>5 degrees angulation * Osteophyte formation of facet joints or vertebral endplates * Decreased disc height, on average by \>2mm, but dependent upon the spinal level * Herniated nucleus pulposus * Facet joint degeneration/changes Exclusion Criteria: 1. Subject is under 18 years of age at the time of consent 2. Subject has had prior lumbar spine fusion surgery at any level 3. Subject is currently undergoing treatment for malignancy or has undergone treatment for malignancy 4. Subject is pregnant or nursing or planning to become pregnant during the two years (24 months) following arthrodesis 5. Subject has an active (local or systemic) infection or is undergoing adjunctive treatment for infection 6. Subjects under workers compensation or active litigation
About the 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
What is being tested
- OssiMend™ Bioactive Moldable (device)
Sponsor: Collagen Matrix · Participants: 120 · Started: Jan 21, 2021
Contact the study team
- Meenakshi Paliwal · Phone: 12014051477
- Peggy Hansen · Phone: 201-405-1477
Official record on ClinicalTrials.gov — NCT04775537
Locations in the U.S.
| California | San Diego Neurosurgery, Encinitas (Not yet recruiting) |
| Connecticut | Hartford Hospital, Hartford |
| New Jersey | University Orthopaedic Associates, Division of OrthoNJ, Somerset (Not yet recruiting) |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.