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Clinical Trial Summary

The primary objective of this study is to demonstrate any changes in assessments of pain for patients receiving Synvisc-One compared to control.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01618708
Study type Interventional
Source Sanofi
Contact
Status Completed
Phase N/A
Start date September 2012
Completion date June 2015

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