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Clinical Trial Summary

Gene therapy is a promising strategy to treat hearing loss and vestibular disorders, and Associated adenovirus (AAV) is shown as a good viral vector for inner ear therapy in animal models. This study aims to study in vitro viral transduction of AAV in human inner ear cells, collected during non-conservative surgeries for vestibular schwannoma.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03996824
Study type Observational
Source Institut Pasteur
Contact Ghizlene Lahlou
Phone 33 1 45688891
Email ghizlene.lahlou@pasteur.fr
Status Recruiting
Phase
Start date February 19, 2019
Completion date February 18, 2027

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