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Study identifier: NCT06485206 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Evaluation of Safety and Effectiveness of Primary Hybrid Construct of Mobi-C and ACDF in the Treatment of Two-level Symptomatic Degenerative Disc Disease in the Cervical Spine.

Condition: Degenerative Disc Disease  ·  Sponsor: Highridge Medical

PhaseNA
Planned participants97
Who can joinAll sexes, 22 Years to 69 Years
Healthy volunteersNo

About this study

The study is a prospective, multi-center cohort study of patients with two-level DDD implanted with CDA adjacent to ACDF (hybrid construct). The overall success of the hybrid procedure will be compared to 2-level ACDF historical controls from the Mobi-C IDE trial. 97 patients will receive the hybrid surgery and will be followed for a minimum of 2 years.

This description comes directly from the study's public registry record.

Talk to the study team

Monica Barascout, BA  ·  1-720-894-9016  ·  monica.barascout@highridgemedical.com

Alex Pawlowski  ·  1-720-894-9016  ·  alex.pawlowski@highridgemedical.com

Always discuss trial participation with your own doctor first.

Locations (2)

University of California-DavisSacramento, California, United StatesRecruiting
Michigan Orthopaedic SurgeonsSouthfield, Michigan, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06485206