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

Enrolling by invitation

Conditions studied: Cervical Disc Disease

In brief

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

Key facts

Study ID

NCT06240221

Run by

Research Source

People needed

200

Starts

2024-04-04

Expected to finish

2028-01-01

Last updated by the study team

2025-08-22

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• 18 years of age or older
• Planned treatment with the Saber-C implant
• Subject is willing and able to sign informed consent

You may not qualify if…

• Subject is pregnant
• Subject is a prisoner

Where it is running

• Strenge Spine — Paducah, Kentucky, United States

Full record on ClinicalTrials.gov

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