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Clinical Trial Summary

This study is designed to evaluate the feasibility of recombinant human bone morphogenetic protein-2 and absorbable collagen sponge with the tapered interbody fusion device (LT-CAGE® ) for anterior lumbar interbody fusion in patients with degenerative disc disease.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01491373
Study type Interventional
Source Medtronic Spinal and Biologics
Contact
Status Completed
Phase N/A
Start date January 1997
Completion date September 1999

See also
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Completed NCT00943384 - Prospective, Multi-Center Clinical Outcomes Study Evaluating the chronOS Strip Combined With Bone Marrow Aspirate N/A
Completed NCT00764491 - OptiMesh® for Lumbar Interbody Fusion Trial (OLIF) N/A
Completed NCT01549366 - Comparison of the Aspen Device Versus Pedicle Screws for Supplemental Posterior Fixation in Lumbar Interbody Fusion N/A
Terminated NCT01980576 - Qualitative Pain Measurement at Patients With Degenerative Low Back Pain N/A
Recruiting NCT02763956 - RCT Study of the Gelstix™ Device to Treat Chronic Discogenic Low Back Pain GelStix Study N/A