At a glance
ClinicalIndex Comparison RecordN/ACompleted· 368 enrolled
Drug / intervention
Total Disc Replacement +1 moredevice
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.
A Multi-Center, Prospective, Randomized, Controlled Clinical Trial Comparing the Safety and Effectiveness of ProDisc-C to Anterior Cervical Discectomy and Fusion (ACDF) Surgery in the Treatment of Symptomatic Cervical Disc Disease (SCDD)
In Brief
A clinical study evaluating Total Disc Replacement and ACDF for Symptomatic Cervical Disc Disease. Completed, enrolled 368 participants.
Detailed Summary
The objective of this clinical investigation is to compare the safety and effectiveness of ProDisc-C to anterior cervical discectomy and fusion (ACDF) surgery in the treatment of symptomatic cervical disc disease (SCDD).
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsSymptomatic Cervical Disc Disease
Countries--
Collaborators--
Timeline
N/ACompletedFinished
2003200420052006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
Enrollment StartAug 2003
First PostedFeb 2006
Primary CompletionMar 2015
TodayJul 2026
First PostedFeb 13, 2006
Enrollment StartAug 1, 2003
Primary CompletionMar 1, 2015
TodayJul 2, 2026
Enrollment to primary: 11.6 yearsPosted 20.4 years ago
Interventions
Total Disc Replacementdevice
Total Disc Replacement using ProDisc-C
ACDFdevice
Anterior Cervical Discectomy and Fusion