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Allograft Tissue

Nucel treatment group for Degenerative Disc Disease

N/A
Waitlist Available
Led By Pierce Nunley, MD
Research Sponsored by Organogenesis
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 2 years
Awards & highlights

Study Summary

This trial looks at whether a certain allograft tissue is safe and effective to use in lumbar interbody fusion procedures.

Eligible Conditions
  • Degenerative Disc Disease
  • Spondylolisthesis
  • Spondylosis

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~2 years
This trial's timeline: 3 weeks for screening, Varies for treatment, and 2 years for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Fusion rate using non-contrast CT of the lumbar spine
Other outcome measures
Neurologic Exam
Oswestry Low Back Pain Disability Index
SF-12 health survey
+1 more

Trial Design

1Treatment groups
Experimental Treatment
Group I: Nucel treatment groupExperimental Treatment2 Interventions
One or two level lumbar interbody fusion surgery with Nucel

Find a Location

Who is running the clinical trial?

OrganogenesisLead Sponsor
35 Previous Clinical Trials
4,070 Total Patients Enrolled
Pierce Nunley, MDPrincipal InvestigatorSpine Institute of Louisiana
1 Previous Clinical Trials
135 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Recent research and studies
clinicaltrials.govStudy
Study of Nucel for One and Two Level Lumbar Interbody Fusion
2015. "Study of Nucel for One and Two Level Lumbar Interbody Fusion". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT02808234.
~21 spots leftby Apr 2025
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