By InvitationNot Applicable

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

United States200 participantsStarted 2024-04-04

Plain-language summary

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

Who can participate

Age range18 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * 18 years of age or older * Planned treatment with the Saber-C implant * Subject is willing and able to sign informed consent Exclusion Criteria: * Subject is pregnant * Subject is a prisoner

What they're measuring

Cervical spinal fusion status assessed via X-rays and CT scans

Timeframe: 1 year

Clinical outcome via neck visual analog scale (VAS)

Timeframe: 1 year

Clinical outcome via neck disability index (NDI)

Timeframe: 1 year

Trial details

NCT IDNCT06240221

SponsorResearch Source

Sponsor typeNETWORK

Study typeOBSERVATIONAL

Primary completion2027-01-01

View on ClinicalTrials.gov More Cervical Disc Disease trials