This study is being done to prospectively collect data on subjects having posterior cervical fusion surgery using the Medtronic Infinity system. Researchers plan to collect information from patients having this type of surgery in order to learn more about patient how patients do after the surgery, including the rate of bone healing following surgery. The goal is for 250 patients to take part in the study or for 500 screws to be used, whichever comes first. Each patient will need a varying amount of screws to be used during their surgery. Because we are measuring the accuracy of each individual screw and the surgeon will likely use multiple screws during each surgery, it is likely that the study will reach its goal of 500 screws before 250 patients are enrolled in the study.
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Related Adverse Events
Timeframe: 49 Days
Upper and Lower Extremity Motor Exam
Timeframe: 49 Days
Sensory Function
Timeframe: 49 Days
Reflexes Score
Timeframe: 49 Days
PROMIS - 29 Profile v2.0 Physical Functioning Subscore
Timeframe: 49 Days
PROMIS - 29 Profile v2.0 Ability to Participate Subscore
Timeframe: 49 Days
PROMIS - 29 Profile v2.0 Anxiety Subscore
Timeframe: 49 Days
PROMIS - 29 Profile v2.0 Depression Subscore
Timeframe: 49 Days
PROMIS - 29 Profile v2.0 Fatigue Subscore
Timeframe: 49 Days
PROMIS - 29 Profile v2.0 Sleep Subscore
Timeframe: 49 Days
PROMIS - 29 Profile v2.0 Pain Intensity Subscore
Timeframe: 49 Days
Cervical Sagittal Alignment
Timeframe: 49 Days
Hoffmann's Response Test
Timeframe: 49 Days
Spurling's Compression Test
Timeframe: 49 Days
All Adverse Events
Timeframe: 49 Days