Trials / Enrolling By Invitation
Enrolling By InvitationNCT06415136
Adjacent Level Anterior Cervical Fusion: SeaSpine Shoreline Versus Removal of Previously Implanted Plate and Replating
- Status
- Enrolling By Invitation
- Phase
- —
- Study type
- Observational
- Enrollment
- 40 (estimated)
- Sponsor
- Research Source · Network
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Accepted
Summary
The purpose of this study is to evaluate the efficacy of SeaSpine Shoreline device in surgery of the cervical spine.
Detailed description
This is a retrospective, prospective, post-market, observational, single-center, single surgeon study evaluating the use of the SeaSpine Shoreline device. Patients will be identified by the Investigator as needing, or already received the device during a cervical fusion surgery and meeting all the inclusion and none of the exclusion criteria.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | SeaSpine Shoreline | The SeaSpine Shoreline device is a minimally invasive cervical plate/cage system. |
Timeline
- Start date
- 2023-05-05
- Primary completion
- 2027-05-01
- Completion
- 2027-05-01
- First posted
- 2024-05-16
- Last updated
- 2025-08-22
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT06415136. Inclusion in this directory is not an endorsement.