Audio-vestibular Evaluation of Children and Young Adults With Osteogenesis Imperfecta
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Could this be for you?
Answer for yourself. This is not a decision: only the study team can say whether you can take part.
- Are you between 12 and 20 years old?
Source: NCT05419960, who can take part
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Contact the study team: see the registry record → Contacts and Locations
Print a page for my doctorTrial details
- Who runs it
- Assistance Publique - Hôpitaux de Paris
- Trial code
- NCT05419960
- Record updated
- 12 September 2025
- Original description
The aim is to determine whether vestibular deficits are present in OI, then to establish whether a correlation exists between genetic type, severity of OI and audiovestibular phenotype. OI patients aged 12 to 20 years will undergo an audiometric, immittance, and vestibular assessment. When hearing loss is conductive or mixed or in cases where vestibular deficits are identified, a CT scan without injection will be performed. In case of sensorineural hearing loss or abnormal CT results, an MRI will be performed.Read full original descriptionShow less
The aim is to determine whether vestibular deficits are present in OI, then to establish whether a correlation exists between genetic type, severity of OI and audiovestibular phenotype. OI patients aged 12 to 20 years will undergo an audiometric, immittance, and vestibular assessment. When hearing loss is conductive or mixed or in cases where vestibular deficits are identified, a CT scan without injection will be performed. In case of sensorineural hearing loss or abnormal CT results, an MRI will be performed.
Inclusion: Patients between the ages of 12-20 years at the time of inclusion; Diagnosis of Osteogenesis Imperfecta of any type; Currently followed by a physician at the CRMR OI; Information and non-opposition of major patients, holders of parental authority and minor patients to participate in the study.
Exclusion: Ophthalmologic pathologies e.g. strabism or severe refraction disorder; Patients with hearing loss of alternate origin e.g. Cochlear nerve deficiency, atresia, etc; Neurological or developmental deficits limiting participation; Cervico-occipital instability e.g. Chiari's malformation; Limitations in mobility of the spine e.g. scoliosis, spinal fractural fusion; Patients under AME (State Medical Aid); Protected adult patients, adults unable to express their consent, pregnant or breastfeeding women.