At a glance
ClinicalIndex Comparison RecordN/ACompleted· 231 enrolled
Drug / intervention
Vectra-Tdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Prospective Multi-Center Clinical Study of Patients With Degenerative Disc Disease Treated With Anterior Cervical Decompression and Fusion Using the Vectra-T Translational Cervical Plate.
In Brief
An observational study evaluating Vectra-T for Degenerative Disc Disease. Completed, enrolled 231 participants across 13 sites.
Detailed Summary
The purpose of this study is to measure the benefits of anterior (from the front) cervical (neck) surgery for degenerative disc disease. The research part of this study is the answering of questionnaires by the patient concerning their quality of life, prior to, and after surgery.
Study Details
Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsDegenerative Disc Disease
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
2006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
Enrollment StartMar 2006
First PostedMar 2007
Primary CompletionApr 2011
TodayJul 2026
First PostedMar 6, 2007
Enrollment StartMar 1, 2006
Primary CompletionApr 1, 2011
TodayJul 2, 2026
Enrollment to primary: 5.1 yearsPosted 19.3 years ago
Interventions
Vectra-Tdevice
Patient will receive the Vectra-T plate (Sized 1 to 4 levels)