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

Part of paid clinical trials in Paducah, Kentucky.

Sponsor
Research Source
Study ID
NCT06240221
Status
Enrolling By Invitation

Conditions

  • Cervical Disc Disease

Eligibility Criteria

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

Interventions

  • Elevation Spine Saber-C System — DEVICE
    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.

Study Details

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

Key Dates

Start date
Apr 4, 2024
Status verified
Aug 2025
Primary completion
Jan 1, 2027
Completion
Jan 1, 2028

Study Design

Enrollment
200 participants (estimated)

Arms

  • Arm: Saber-C
    All enrolled patients will receive the Elevation Spine Saber-C System according to surgeon standard of care.

Primary Outcome Measure

Cervical spinal fusion status assessed via X-rays and CT scans [ Time Frame: 1 year ]

Locations (1)

FacilityCityStateZIPSite coordinators
Strenge SpinePaducahKentucky42003-

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Strenge Spine· Paducah, KY

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