Safety and Efficacy Study Comparing ProDisc-C to ACDF Surgery to Treat SCDD

Symptomatic Cervical Disc Disease Clinical Trial

Official title:
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)

Status Completed

Clinical Trial 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).

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT00291018
Study type	Interventional
Source	Synthes USA HQ, Inc.
Contact
Status	Completed
Phase	N/A
Start date	August 1, 2003
Completion date	March 1, 2015

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See also
Status	Clinical Trial	Phase
Completed	`NCT00882661` - SECURE®-C Cervical Artificial Disc Clinical Study/ SECURE-C Cervical Artificial Disc Postmarket Approval Study	N/A
Completed	`NCT00758758` - Performance of the Hedrocel(R) Cervical Fusion Device	Phase 3
Not yet recruiting	`NCT04167878` - Exploratory Study of 3D Printed Biodegradable Cervical Interbody Fusion Cage	N/A
Recruiting	`NCT04012996` - 2-level Cervical Disc Replacement Comparing Prodisc C SK & Vivo to Mobi-C	N/A
Not yet recruiting	`NCT05610397` - Retrospective Study With Patients Treated With STALIF® C or M and Ti or FLX Implants for 1 and 2 Levels
Terminated	`NCT03828136` - Novum Vitrium® Cervical Cage in Anterior Cervical Discectomy and Fusion	N/A