This study aims to determine to what extent patient-specific factors, iatrogenic factors, and
biomechanical factors influence cervical spine mechanics after single-level and two-level
Procedure: C5-C6 arthrodesis
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Full eligibility criteria for NCT03028402
Ages eligible for Study
21 Years to 60 Years
Genders eligible for Study
Accepts Healthy Volunteers
Patients must agree to return for all follow-up visits and provide informed consent.
Control subjects will be asymptomatic, with no injury or disease that will interfere with spine function, such as previous spine surgery or trauma.
Participants will have no other injury or disease that will interfere with spine function, such as previous spine surgery or trauma
Individuals who have been previously clinically diagnosed with poor bone quality and those who do not intend to stay in the Pittsburgh area for a period of at least 3 years post-surgery will be excluded.
Females who are pregnant or plan to be pregnant within 3 years of surgery will be excluded.
All locations for NCT03028402
United States (1)
University of Pittsburgh Biodynamics Lab
Pittsburgh, Pennsylvania, United States, 15203
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Tris trial is registered with FDA with number: NCT03028402. The sponsor of the trial is University of Pittsburgh and it is looking for 110 volunteers for the current phase.
Official trial title: Adjacent Segment Mechanics in Cervical Arthrodesis Patients
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