Adjacent Level Anterior Cervical Fusion: SeaSpine Shoreline Versus Removal of Previously Implanted Plate and Replating
NCT06415136 · Status: ENROLLING_BY_INVITATION · Type: OBSERVATIONAL · Enrollment: 40
Last updated 2025-08-22
Summary
The purpose of this study is to evaluate the efficacy of SeaSpine Shoreline device in surgery of the cervical spine.
Conditions
- Degenerative Disc Disease
- Disc Herniation
Interventions
- DEVICE
-
SeaSpine Shoreline
The SeaSpine Shoreline device is a minimally invasive cervical plate/cage system.
Sponsors & Collaborators
-
Research Source
lead NETWORK
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2023-05-05
- Primary Completion
- 2027-05-31
- Completion
- 2027-05-31
- FDA Device
- Yes
Countries
- United States
Study Locations
More Related Trials
-
Cervical I/F Cage for Anterior Cervical Fusion
NCT00215293 ·Status: COMPLETED ·Phase: PHASE3
-
Prospective Study of Fusion Rates Using Spira-C Device for Anterior Cervical Discectomy and Fusion Surgery
NCT03786432 ·Status: TERMINATED ·Phase: NA
-
Study Using the CervicalStim Device Following Cervical Fusion
NCT03177473 ·Status: COMPLETED
-
Cervical Interbody Fusion Device Patient Registry
NCT05114356 ·Status: TERMINATED
-
M6-C Artificial Cervical Disc Two-Level IDE Pivotal Study
NCT04982835 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
CEM-Plate and CEM-Cage First-In-Human Use Efficacy Study
NCT04883411 ·Status: RECRUITING ·Phase: NA
-
Assessing Safety of Cervical Spine Fusion With NMP®
NCT07245940 ·Status: NOT_YET_RECRUITING
-
Evaluation of Cervical Fusion With DTRAX® Cervical Cage With DTRAX Bone Screw
NCT02694250 ·Status: WITHDRAWN ·Phase: NA
-
Cervical Spondylotic Myelopathy Surgical Trial
NCT02076113 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
Effectiveness and Safety of Mobile Artificial Cervical Vertebrae Replacement for Patients With Cervical Spondylosis
NCT04813211 ·Status: UNKNOWN ·Phase: NA
-
Total Disc Replacement Versus Anterior Cervical Decompression and Fusion
NCT02417272 ·Status: COMPLETED ·Phase: NA
-
Investigation of DEXA-C Anterior Cervical Interbody System
NCT05883436 ·Status: RECRUITING ·Phase: NA
-
Safety and Performance of the SPINEVISION Hexanium ACIF in the Treatment of Cervical Spine Degenerative Disc Disease
NCT06155409 ·Status: ACTIVE_NOT_RECRUITING
-
A Clinical Registry to Track the Real World Use of the Saber-C® Cervical Fusion Device
NCT06240221 ·Status: ENROLLING_BY_INVITATION
-
Advent™ Cervical Disc Versus ACDF for Treatment of One Level Degenerative Disc Disease (IDE Study)
NCT00637312 ·Status: TERMINATED ·Phase: NA
-
A Retrospective Study to Examine the Effect of CMF Stimulation on Primary ACDF Patients
NCT05101057 ·Status: UNKNOWN
-
Posterior Cervical Fixation Study
NCT04770571 ·Status: ENROLLING_BY_INVITATION
-
Comparison of DISCOVER™ Artificial Cervical Disc and ACDF for Treatment of Cervical DDD (IDE Study)
NCT00432159 ·Status: COMPLETED ·Phase: NA
-
Investigation of the Two Level Simplify® Cervical Artificial Disc
NCT03123549 ·Status: COMPLETED ·Phase: NA
-
The Synergy Disc To Anterior Cervical Discectomy and Fusion
NCT04469231 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
Adjacent Segment Mechanics in Cervical Arthrodesis Patients
NCT03028402 ·Status: COMPLETED
-
Instr. vs. Non-instr. Posterolateral Spinal Fusion in Patients With Spinal Stenosis and Degenerative Listhesis
NCT04166981 ·Status: COMPLETED ·Phase: NA
-
Radiographic and Clinical Evaluation of Surgical Treatment for Cervical Deformity: A Multi-Center Study 2.0
NCT04194996 ·Status: RECRUITING
-
A Study of Korean Society of Spine Surgery on the Outcomes of Anterior Cervical Discectomy and Fusion
NCT01911013 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
Stand-Alone Cage Verus Anterior Plating for Anterior Cervical Discectomy and Fusion.
NCT03312192 ·Status: WITHDRAWN ·Phase: NA