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

Part of paid clinical trials in Southfield, Michigan.

Sponsor
Research Source
Study ID
NCT06415136
Status
Enrolling By Invitation

Conditions

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Accepted

Interventions

  • SeaSpine Shoreline — DEVICE
    The SeaSpine Shoreline device is a minimally invasive cervical plate/cage system.

Study Details

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

Key Dates

Start date
May 5, 2023
Status verified
Aug 2025
Primary completion
May 31, 2027
Completion
May 31, 2027

Study Design

Enrollment
40 participants (estimated)

Arms

  • Arm: SeaSpine Shoreline
    All enrolled patients will receive the SeaSpine Shoreline device.

Primary Outcome Measure

Cervical fusion assessed via CT scan [ Time Frame: 12 months post surgery ]

Locations (1)

FacilityCityStateZIPSite coordinators
Michigan Orthopaedic SurgeonsSouthfieldMichigan48033-

Find similar trials in Southfield, MI

By research site
Michigan Orthopaedic Surgeons· Southfield, MI

Related Studies