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Single-Armed Use of ViviGen Cellular Bone Matrix in Patients Undergoing Posterolateral Lumbar Surgery

A Prospective, Single Arm Study of Patients Undergoing Posterolateral Lumbar Fusion (Without Interbody) Supplemented With ViviGen Cellular Bone Matrix

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04007094
Enrollment
21
Registered
2019-07-05
Start date
2019-02-12
Completion date
2022-01-21
Last updated
2024-01-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Degenerative Disc Disease, Spinal Stenosis, Spondylolisthesis, Spondylosis

Brief summary

This is a prospective, single-arm post market study of patients to assess fusion in one or multiple continuous levels of the lumbosacral spine (L1-S1) using ViviGen Cellular Bone Matrix. All subjects will be followed out to 24 months for final assessment.

Detailed description

Lumbar spine fusion rates can vary according to the surgical technique. Although many studies on spinal fusion have been conducted and reported, the heterogeneity of the study designs and data handling make it difficult to identify which approach yields the highest fusion rate. Traditional posterolateral intertransverse fusion (PLF) still remains a good procedure with acceptable fusion rates for most degenerative conditions. For solid fusion, PLF can be combined with interbody fusion to circumferentially stabilize the relevant segment, even though it is unclear whether this improves fusion rates. A bone graft or bone graft substitute is required to produce the fusion and can be implanted on its own, in the posterolateral gutters, or contained with an interbody device using either a posterior or anterior approach. Spinal laminectomy is most often the largest generator of bone graft product due to the nature of the procedure. The current gold standard is autograft bone, in which tissue is harvested locally or from the iliac crest and is then placed at the site. However, local bone graft may be relatively limited and harvesting at the iliac crest can easily lead to significant morbidity. Complications such as inflammation, infection, and chronic pain may outlast the pain of the original surgical procedure. Autograft is the gold standard because it possesses all of the characteristics necessary for new bone growth-namely, osteoconductivity, osteogenicity, and osteoinductivity. Allograft tissues are alternatives to autografts and are taken from donors or cadavers, circumventing some of the shortcomings of autografts by eliminating donor-site morbidity and issues of limited supply. Osteoconductivity refers to the situation in which the graft supports the attachment of new osteoblasts and osteoprogenitor cells, providing an interconnected structure through which new cells can migrate and new vessels can form. Osteogenicity refers to the situation when the osteoblasts that are at the site of new bone formation are able to produce minerals to calcify the collagen matrix that forms the substrate for new bone. Osteoinductivity refers to the ability of a graft to induce nondifferentiated stem cells or osteoprogenitor cells to differentiate into osteoblasts. Using the 2 basic criteria of a successful graft, osteoconduction and osteoinduction, investigators have developed several alternatives, some of which are available for clinical use and others of which are still in the developmental stage. Many of these alternatives use a variety of materials, including natural and synthetic polymers, ceramics, and composites, whereas others have incorporated factor- and cell-based strategies that are used either alone or in combination with other materials.

Interventions

ViviGen Cellular Bone Matrix is a formulation of cryopreserved viable cortical cancellous bone matrix and demineralized bone. ViviGen is a Human Cells, Tissues, and Cellular and Tissue-based Product (HCT/P) as defined by the U.S. Food and Drug Administration in 21 CFR 1271.10

Sponsors

DePuy Synthes
CollaboratorINDUSTRY
Ohio State University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Subject is scheduled to undergo a single or multilevel posterolateral spinal fusion surgery using ViviGen Cellular Bone matrix * Subject must be over the age of 18 years old * Subject has been unresponsive to conservative care for a minimum of 6 months. * The subject must in the investigator's opinion, be psychosocially, mentally, and physically able to fully comply with this protocol including the required follow-up visits, the filling out of required forms, and have the ability to understand and give written informed consent.

Exclusion criteria

* Subjects requiring additional bone grafting materials other than local autograft and ViviGen Cellular Bone Matrix will be excluded from this outcomes study. * Subject has inadequate tissue coverage over the operative site * Subject has an open wound local to the operative area, or rapid joint disease, bone absorption, or osteoporosis. * Subject has a condition requiring medications that may interfere with bone or soft tissue healing (i.e., oral or parenteral glucocorticoids, immunosuppressives, methotrexate, etc.). * Subject has an active local or systemic infection. * Subject has a metal sensitivity/foreign body sensitivity. * Subject is morbidly obese, defined as a body mass index (BMI) greater than 45. * Subject has any medical condition or extenuating circumstance that, in the opinion of the investigator, would preclude participation in the study. * Subject is currently involved in another investigational drug or device study that could confound study data. * Subject has a history (present or past) of substance abuse (recreational drugs, prescription drugs or alcohol) that in the investigator's opinion may interfere with protocol assessments and/or with the subject's ability to complete the protocol required follow-up. * Subjects who are pregnant or plan to become pregnant in the next 24 months or who are lactating. * Subject is involved in or planning to engage in litigation or receiving Worker's Compensation related to neck or back pain. * Osteoporosis (per the investigator's diagnosis or per a T-score \> 2.5 standard deviations below the mean for a young, healthy adult) that may prevent adequate fixation of screws and thus preclude the use of a pedicle screw system. * Subjects who have a known or suspected allergy to any of the following antibiotics and/or reagents: Gentamicin Sulfate, Meropenem, Vancomycin, Dimethyl Sulfoxide (DMSO), and Human Serum Albumin (HSA); * Immune compromised subjects * Known sensitivity to device materials * Subject is a prisoner.

Design outcomes

Primary

MeasureTime frameDescription
The Number of Surgical Levels With Successful Lumbar Fusion12 months prospective from surgeryExtent of fusion using the Lenke classification. Radiographic success defined as grade A, partial success grade B and radiographic failure as grades C and D.

Secondary

MeasureTime frameDescription
Number of Participants With or Without Changes in Visual Analog Scale Pain Scores12 months prospectively from surgeryThe visual analog scale will be used to rate leg and back pain scores from 0-10, with 10 being considered the most painful.
Oswestry Disability Index (ODI) v2.1a12 months prospectively from surgeryThis survey will be used to assess how back pain affects patients' ability to function in everyday life. We will look to see if subjects' scores improve or worsen on the Oswestry Disability Index scale (ODI) which can range from 0% to 100% with higher scores indicating higher levels of disturbance in everyday life.

Countries

United States

Participant flow

Participants by arm

ArmCount
Study Arm
Participants will be entered into the single armed study in which one side of the fusion will be coated with milled local autograft bone and the opposite fusion side will be supplemented with an equal volume of Depuy Synthes ViviGen. ViviGen Cellular Bone Matrix: Study participants will receive local autograft milled bone on one side of the fusion and an equal amount of Depuy Synthes ViviGen on the opposite side of the fusion
21
Total21

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyLost to Follow-up11

Baseline characteristics

CharacteristicStudy Arm
Age, Categorical
<=18 years
0 Participants
Age, Categorical
>=65 years
16 Participants
Age, Categorical
Between 18 and 65 years
5 Participants
Age, Continuous70.95 years
STANDARD_DEVIATION 9.34
Ethnicity (NIH/OMB)
Hispanic or Latino
0 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
21 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants
Race (NIH/OMB)
Asian
0 Participants
Race (NIH/OMB)
Black or African American
2 Participants
Race (NIH/OMB)
More than one race
0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants
Race (NIH/OMB)
Unknown or Not Reported
1 Participants
Race (NIH/OMB)
White
18 Participants
Region of Enrollment
United States
21 participants
Sex: Female, Male
Female
9 Participants
Sex: Female, Male
Male
12 Participants

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
0 / 21
other
Total, other adverse events
14 / 21
serious
Total, serious adverse events
6 / 21

Outcome results

Primary

The Number of Surgical Levels With Successful Lumbar Fusion

Extent of fusion using the Lenke classification. Radiographic success defined as grade A, partial success grade B and radiographic failure as grades C and D.

Time frame: 12 months prospective from surgery

Population: Surgical Levels have two sides being evaluated: 55 levels times 2: (Left- Autograft and Right - ViviGen)

ArmMeasureGroupValue (NUMBER)
Left Side - Milled Local Autograft BoneThe Number of Surgical Levels With Successful Lumbar FusionGrade A24 Surgical Levels
Left Side - Milled Local Autograft BoneThe Number of Surgical Levels With Successful Lumbar FusionGrade B14 Surgical Levels
Left Side - Milled Local Autograft BoneThe Number of Surgical Levels With Successful Lumbar FusionGrade C15 Surgical Levels
Left Side - Milled Local Autograft BoneThe Number of Surgical Levels With Successful Lumbar FusionGrade D2 Surgical Levels
Right Side - Depuy Synthes ViviGenThe Number of Surgical Levels With Successful Lumbar FusionGrade D0 Surgical Levels
Right Side - Depuy Synthes ViviGenThe Number of Surgical Levels With Successful Lumbar FusionGrade A34 Surgical Levels
Right Side - Depuy Synthes ViviGenThe Number of Surgical Levels With Successful Lumbar FusionGrade C12 Surgical Levels
Right Side - Depuy Synthes ViviGenThe Number of Surgical Levels With Successful Lumbar FusionGrade B9 Surgical Levels
Secondary

Number of Participants With or Without Changes in Visual Analog Scale Pain Scores

The visual analog scale will be used to rate leg and back pain scores from 0-10, with 10 being considered the most painful.

Time frame: 12 months prospectively from surgery

ArmMeasureGroupValue (NUMBER)
Left Side - Milled Local Autograft BoneNumber of Participants With or Without Changes in Visual Analog Scale Pain ScoresBack Pain Scores Improved on Scale12 participants
Left Side - Milled Local Autograft BoneNumber of Participants With or Without Changes in Visual Analog Scale Pain ScoresLeg Pain Scores Improved on Scale11 participants
Left Side - Milled Local Autograft BoneNumber of Participants With or Without Changes in Visual Analog Scale Pain ScoresBack Pain Scores Worsened on Scale2 participants
Left Side - Milled Local Autograft BoneNumber of Participants With or Without Changes in Visual Analog Scale Pain ScoresLeg Pain Score Worsened on Scale1 participants
Left Side - Milled Local Autograft BoneNumber of Participants With or Without Changes in Visual Analog Scale Pain ScoresBack Pain Score did not change2 participants
Left Side - Milled Local Autograft BoneNumber of Participants With or Without Changes in Visual Analog Scale Pain ScoresLeg Pain Score did not change3 participants
Left Side - Milled Local Autograft BoneNumber of Participants With or Without Changes in Visual Analog Scale Pain ScoresBack Pain Change Unknown/Unreported4 participants
Left Side - Milled Local Autograft BoneNumber of Participants With or Without Changes in Visual Analog Scale Pain ScoresLeg Pain Change Unknown/Unreported5 participants
Secondary

Oswestry Disability Index (ODI) v2.1a

This survey will be used to assess how back pain affects patients' ability to function in everyday life. We will look to see if subjects' scores improve or worsen on the Oswestry Disability Index scale (ODI) which can range from 0% to 100% with higher scores indicating higher levels of disturbance in everyday life.

Time frame: 12 months prospectively from surgery

ArmMeasureGroupValue (NUMBER)
Left Side - Milled Local Autograft BoneOswestry Disability Index (ODI) v2.1aOswestry Disability Index Score Improved9 participants
Left Side - Milled Local Autograft BoneOswestry Disability Index (ODI) v2.1aOswestry Disability Index Score Worsened3 participants
Left Side - Milled Local Autograft BoneOswestry Disability Index (ODI) v2.1aOswestry Disability Index Score did not Change1 participants
Left Side - Milled Local Autograft BoneOswestry Disability Index (ODI) v2.1aOswestry Disability Index Score Unknown/Not Reported7 participants

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026