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Clinical Trial Summary

This study evaluates a medialization implant to treat vocal cord paralysis, to permit it to adjust the quality of the voice under local or general anesthesia. The aim is to restore phonation using a porous titanium prosthesis in laryngeal surgery.


Clinical Trial Description

n/a


Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00213863
Study type Interventional
Source University Hospital, Strasbourg, France
Contact Christian Debry, MD
Email christian.debry@chru-strasbourg.fr
Status Recruiting
Phase Phase 2
Start date December 2010
Completion date November 2016

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