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Evaluation on Efficacy of Total Artificial Disc Replacement (TDR) of Cervical Spondylosis

Cervical Spondylosis Clinical Trial

Official title:
Evaluation on Efficacy of Total Artificial Disc Replacement (TDR) of Cervical Spondylosis: a Cohort Prospective Follow-up for 5 Years

Clinical Trial Summary

To evaluate the efficacy of 3 different types of cervical disc prosthesis (Prodisc-C, Mobi-C and Prestige-LP) in the treatment of cervical spondylosis.

Clinical Trial Description

A cohort, retrospective analysis will be performed of 150 patients who were in implementation of artificial disc replacement in our department from 2008 to 2012 and accepted a regular postoperatively follow-up up to 5 years, the sample will be divided into 3 groups according to prosthesis and 50 people in each group. The outcome will be measured among 3 groups respectively on the operation (such as operation time, intraoperative bleeding.), postoperative complications (such as prosthesis sinking, displacement and prolapse, adjacent segments degeneration and heterotopic ossification), photographic indicators and functional efficacy analysis and then a comparison for self-contrast pre- and post-operatively. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03364816
Study type Observational
Source Peking University People's Hospital
Contact Shuai Xu
Phone (86)18811792718
Email 1204649202@qq.com
Status Not yet recruiting
Phase N/A
Start date February 1, 2018
Completion date December 31, 2018
View Details
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