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PASS MIS® Post-market Clinical Follow-up

Spinal Fractures Clinical Trial

Official title:
Evaluation of the Efficacy and Safety of the PASS MIS® System in the Treatment of Spinal Thoracolumbar Fractures

Clinical Trial Summary

Prospective, multicenter non comparative and observational study (post-market clinical follow-up).

Clinical Trial Description

Patients operated with PASS MIS® manufactured by MEDICREA® INTERNATIONAL between July 2016 and July 2017. The inclusion period will be 12 months and the follow-up 24 months ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02931266
Study type Observational
Source Medicrea International
Contact
Status Terminated
Phase
Start date September 2016
Completion date January 2018
View Details
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