Research Source
The objective of this study is to collect clinical and radiographic outcomes using the CONDUIT™ Interbody Cervical System with supplemental fixation using a DePuy Synthes Cervical Plating System.
The primary aim of this study is to evaluate the performance of the CONDUITTM Interbody Cervical System in reducing pain and degree of disability as measured using the Neck Disability Index (NDI). Recruitment will occur from the patient population of the investigator. All patients will be evaluated for participation in the study by using the inclusion/exclusion listed below. Subjects need to meet all the inclusion and none of the exclusion. The responsibility is exclusively maintained by the investigator of any potential study participant as defined by the inclusion/ exclusion. Patients will c…
Inclusion Criteria: 1. Male or female subject; at least 18 years of age 2. Diagnosis of radiculopathy or myelopathy with radiculopathy of the cervical spine, with pain, paresthesias or paralysis in a specific nerve root distribution C2 through T1, including at least one of the following: 1. Neck and/or arm pain of at least 30/100 mm on the visual analogue scale (VAS) scale 2. Decreased muscle strength of at least one level on the clinical evaluation (0 to 5) scale 3. Abnormal sensation including hyperesthesia or hypoesthesia; and/or 4. Abnormal reflexes 3. Symptomatic cervical di…
CONDUIT Interbody Cervical System will be inserted between C2 through T1 and fixated using a DePuy Synthes Cervical Plating System at 1 or 2 levels.
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