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Study of an Expandable Interbody Device for the Lumbar Spine — CALIBER  

Degenerative Disc Disease Clinical Trial

Official title:
Efficacy and Safety of Expandable Spacer in the Treatment of Degenerative Disc Disease Using the Minimally Invasive Transforaminal Lumbar Interbody Fusion Surgical Approach

Clinical Trial Summary

The primary objective of this study is to evaluate the safety and efficacy of CALIBER expandable spacer for the treatment of degenerative disc disease. Radiographic outcomes, intra-operative parameters, clinical outcomes, and patient satisfaction will be obtained from patients in this 2 year follow-up clinical study.

Clinical Trial Description

Patients will be followed-up at 3weeks, 6 weeks, 3 months, 6 months, 12 and 24 months with X-rays and questionnaires to determine their satisfaction, healing, fusion and return to work status ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02075554
Study type Interventional
Source Globus Medical Inc
Contact
Status Completed
Phase N/A
Start date July 2012
Completion date February 2017
View Details
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