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Study identifier: NCT06704919 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Conduit Cages and Fibergraft BG Putty

Condition: Degenerative Disc Disease · Herniated Disc  ·  Sponsor: Nitin Agarwal

PhaseN/A
Planned participants100
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The Conduit cages are intended to restore the intervertebral height and to facilitate the intervertebral body fusion in the cervical and lumbar spine in skeletally mature patients with degenerative disc disease and instabilities at one or more levels of the spine. The Fibergraft Bioactive Glass (BG) is engineered to mimic the body's natural bone healing process. While previous studies have described the use of conduit cages in interbody fixation procedures, these studies did not specifically study the clinical and radiographic outcomes of patients who have received these implants in addition to Fibergraft. We aim to recruit patients with degenerative disc disease, and instabilities at one to multilevel contiguous levels between C2-T1 and 1-2 contiguous levels between L2-S1 of the spine with accompanying radicular symptoms, ruptured or herniated discs, and pseudarthrosis and spondylodesis. We will then follow these patients for a duration of two years to report their clinical and radiographic outcomes to determine fusion, complication rate, and revision surgeries if any.

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

Talk to the study team

Nitin Agarwal, MD  ·  9085311947  ·  nitin.agarwal@upmc.edu

Rida Mitha, MD  ·  3147327092  ·  mithar@upmc.edu

Always discuss trial participation with your own doctor first.

Locations (1)

University of Pittsburgh Medical CenterPittsburgh, Pennsylvania, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06704919