Audio-vestibular Evaluation of Children and Young Adults With Osteogenesis Imperfecta

Status: Not yet recruiting
Location: See location...
Intervention Type: Diagnostic Test
Study Type: Observational
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 12
Maximum Age: 20
Healthy Volunteers: No
View:

• 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

Locations
Other Locations
France
Hôpital Necker-Enfants Malades
Paris
Contact Information
Primary
Natalie Loundon, MD, PhD
natalie.loundon@aphp.fr
1 71 39 67 82
Backup
Hélène Morel
helene.morel@aphp.fr
1 71 19 63 46
Time Frame
Start Date: June 2022
Estimated Completion Date: June 2024
Participants
Target number of participants: 44
Treatments
Patients
Patients between the ages of 12-20 years with a diagnosis of Osteogenesis Imperfecta of any type and followed by a physician at the Centre de Référence des Maladies Rares des maladies osseuses constitutionnelles (CRMR OI) of Hôpital Necker-Enfants malades.
Sponsors
Leads: Assistance Publique - Hôpitaux de Paris

This content was sourced from clinicaltrials.gov

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