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A Clinical Registry to Track the Real World Use of the Saber-C® Cervical Fusion Device

Cervical Disc Disease Clinical Trial

Official title:
A Clinical Registry to Track the Real World Use of the Saber-C® Cervical Fusion Device When Used for the Treatment of

Clinical Trial Summary

The objective of this registry study is to collect radiographic and clinical outcome measures to determine the effectiveness of the Saber-C device.

Clinical Trial Description

The purpose of this Clinical Registry is to track the real world use the Saber-C cervical fusion device when used for the treatment of Cervical Degenerative Disc Disease from C-2 to T1 for Anterior Cervical Discectomy and Fusion (ACDF). The registry is intended to profile the use of the Saber-C cervical fusion device when used according to surgeon standard of care at clinical practices throughout the United States. The focus of the registry will be to track and better understand the safety, effectiveness and market value of the Saber-C cervical fusion device. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06240221
Study type Observational [Patient Registry]
Source Research Source
Contact
Status Enrolling by invitation
Phase
Start date April 4, 2024
Completion date January 1, 2028
View Details
See also
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