Otosclerosis Clinical Trial
Official title:
Therapeutic Efficacy of Tiludronic Acid on Inner Ear Involvement in Advanced Otosclerosis
The aim of this study is to assess the efficacy of a biphosphonate (tiludronic acid, Skelid®, Sanofi-Aventis) in the treatment of inner ear involvement in advanced otosclerosis
Otosclerosis is a bone dystrophy localized to middle and inner ears with unknown etiology. It
principally concerns adult patients between 30 and 50 years of age. Women present with this
disease 2 times more frequently than men. Family cases are observed in 50% with a dominant
autosomal transmission and low penetrance (40%). In its early stages, the disease is mainly
located at the stapediovestibular joint leading to its ankylosis and a conductive hearing
loss. In its advanced stages, the lesions extend around the cochlea and vestibule, induce a
sensorineural hearing loss which can progress to severe and profound deafness, and prolonged
balance disorders. On CT-scan, disease foci show a demineralization. Their density is
inversely correlated to the hearing loss. In early stage, hearing function is currently
rehabilitated by conventional hearing aids or surgery. In advanced forms, cochlear
involvement is not accessible to surgery, and rehabilitation is insured by he hearing aids or
cochlear implants. Vestibular dysfunction is dealt with by physiotherapy or symptomatic
treatment. Drugs with anabolic activity in bone, such as sodium fluoride and etidronate
(first generation bisphosphonate, Didronel ®), appear to reduce the hearing loss and to
increase the radiological density of disease foci. However, their efficacy is low and poorly
documented. Their effect on vestibular function is unknown.
Moreover, ototoxicity has been reported for etidronate. New biphosphonates such as tiludronic
acid (Skelid ®) have a significantly more potent inhibition of bone resorption and do not
have an ototoxic effect. They have been used for the treatment or the prevention of
postmenopausal osteoporosis and in Paget's disease with mild to moderate adverse effects in
the majority of cases.
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