Adjacent Level Anterior Cervical Fusion: SeaSpine Shoreline Versus Removal of Previously Implanted Plate and Replating

Enrolling by invitation

Conditions studied: Degenerative Disc Disease, Disc Herniation

In brief

The purpose of this study is to evaluate the efficacy of SeaSpine Shoreline device in surgery of the cervical spine.

Key facts

Study ID

NCT06415136

Run by

Research Source

People needed

40

Starts

2023-05-05

Expected to finish

2027-05-01

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…

• Appropriate patient, as determined by the Investigator, scheduled for an elective cervical spine fusion to treat adjacent level cervical disc herniation or degeneration resulting in cervical radiculopathy or myelopathy
• At least 18 years of age
• Failure of nonoperative care
• Previous anterior cervical plating
• Psychosocially, mentally and physically able to comply with this protocol including adhering to follow-up schedule and study requirements

You may not qualify if…

• Pregnancy or anticipated to become pregnant during the course of the study
• No previous cervical spine surgery
• Non-instrumented cervical fusion
• Cervical fusion with separate plate fixation
• Unwilling or unable to sign consent
• Patient has any condition, that in the opinion of the Investigator, would prohibit the patient from complying with the protocol
• Currently a prisoner

Where it is running

• Michigan Orthopaedic Surgeons — Southfield, Michigan, United States

Full record on ClinicalTrials.gov

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