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Clinical Trial Summary

to compare, the osseous density in the mastoid of two products used to obliterate the mastoid during surgery for cholesteatoma


Clinical Trial Description

Primary objective: To compare the radiological aspect in the petrous bone of two obliteration products in adults, one year after surgery (Bioactive Glass S53P4 and biological Hydroxy apatite) secondary objective : To evaluate the cutaneous and the inner ear tolerance of bioactive glass S53P4 and biological hydroxy apatite when used in the mastoid and epitympanic obliteration for chronic otitis surgery ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05072678
Study type Observational
Source University Hospital, Brest
Contact remi Marianowski, MD, PhD
Phone 33298223333
Email remi.marianowski@chu-brest.fr
Status Recruiting
Phase
Start date April 25, 2021
Completion date April 25, 2023

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