NCT06240221

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

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

• Status: Enrolling By Invitation
• Phase: —
• Study type: Observational
• Enrollment: 200 (estimated)
• Sponsor: Research Source · Network
• Sex: All
• Age: 18 Years
• Healthy volunteers: Accepted

Summary

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

Detailed 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.

Conditions

• Cervical Disc Disease

Interventions

Type	Name	Description
DEVICE	Elevation Spine Saber-C System	Device: Elevation Spine Saber-C System Elevation Spine Saber-C System will be fixated between C2 through T1 according to surgeon standard of care at clinical practices through the United States.

Timeline

• Start date: 2024-04-04
• Primary completion: 2027-01-01
• Completion: 2028-01-01
• First posted: 2024-02-02
• Last updated: 2025-08-22

Locations

1 site across 1 country: United States

Regulatory

• FDA-regulated device study