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

NCT ID: NCT05419960

Last Updated: 2025-09-12

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

RECRUITING

Total Enrollment

44 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-12-22

Study Completion Date

2027-12-22

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Osteogenesis Imperfecta (OI), or Lobstein's disease, is a form of congenital osteoporosis, with a prevalence between 1/10,000 and 1/20,000 in France. As of 1979, four phenotypes have been described according to severity: moderate (type I), lethal (type II), severe (type III), and moderate-to-severe (type IV). OI exhibits phenotypic and genotypic variability, however, to date no correlations have been established between specific mutations and clinical presentation.

There is a well-established association between OI and hearing loss, however, the reported prevalence of hearing loss varies between 2% to 94.1%.

In patients with OI, Computed Tomography (CT) has revealed bone demineralization that progresses with age.

The extent of the hypodense areas on the CT corresponds to the type of hearing loss: conductive hearing loss is associated with lesions of the fissula ante fenestram and round and oval windows while mixed hearing loss is associated with additional retrofenestral lesions. Severity of hearing loss is positively correlated with OI-related bone damage in the petrous bone. Magnetic Resonance Imaging (MRI) has also revealed in the pericochlear lesions with soft tissue hypersignal and enhancement on contrast medium injection in the otic capsule. Bone demineralization has also been linked to vestibular deficits, and some studies have reported correlations between Osteogenesis Imperfecta and vestibular deficits in adult patients, however, this relationship is less clear.

The aim of the study is to determine whether vestibular deficits are also present in OI. Furthermore, the study will aim to establish whether a correlation exists between genetic type, severity of OI and audiovestibular phenotype. OI patients aged 12 to 20 years will be recruited and an audiometric, immittance, and vestibular assessment (videonystagmography, video Head Impulse Test (vHIT), vestibular evoked muscular potentials (cVEMP)) will be performed during their annual visit to the Centre de Référence des Maladies Rares des maladies osseuses constitutionnelles (henceforth CRMR OI) of Hôpital Necker-Enfants malades, Paris, France. When hearing loss is conductive, or mixed or in cases where vestibular deficits are identified, a CT scan without injection will be performed for the care. In case of sensorineural hearing loss, or abnormal CT results, an MRI will be proposed for the care. The investigation team will try to establish if there is a significant association between OI and vestibular deficit, and if so, whether the degree of vestibular impairment is correlated to radiological findings with respect to bone abnormalities, as well as the type and severity of the deafness.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Osteogenesis Imperfecta

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

CASE_ONLY

Study Time Perspective

CROSS_SECTIONAL

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

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.

Vestibular Assessment

Intervention Type DIAGNOSTIC_TEST

During the usual hearing assessment (immittance testing and pure-tone and speech audiometry) carried out by patients, a vestibular assessment will be done for the study to detect vestibular disorders:

* Videonystagmography (VNG) Is the study of eye movement with the help of infrared googles.
* Subjective Visual Vertical (SVV) The patient is asked to orient a line on the vertical axis.
* Video Head Impulse Test (vHIT)
* Cervical and Ocular Vestibular Evoked Myogenic Potential (cVEMP and oVEMP)

Petrous bone Computed Tomography (CT)

Intervention Type DIAGNOSTIC_TEST

For patients diagnosed with hearing loss, whether conductive, mixed, and/or a vestibular deficit, a CT scan (without injection) will be proposed for their care.

Petrous bone Computed Tomography (CT) is an imaging technique used as the standard method of evaluation of the boney structures in the ear.

Magnetic Resonance Imaging (MRI)

Intervention Type DIAGNOSTIC_TEST

Patients that have done a CT and for who CT results was abnormal, will additionally require an MRI for their standard care.

Magnetic Resonance Imaging (MRI) is an imaging technique used as the standard method of evaluation of the cochlear, retrocochlear and central and peripheral nervous system. An injection of Gadolinium contrast media will be used to enhance certain recordings.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Vestibular Assessment

During the usual hearing assessment (immittance testing and pure-tone and speech audiometry) carried out by patients, a vestibular assessment will be done for the study to detect vestibular disorders:

* Videonystagmography (VNG) Is the study of eye movement with the help of infrared googles.
* Subjective Visual Vertical (SVV) The patient is asked to orient a line on the vertical axis.
* Video Head Impulse Test (vHIT)
* Cervical and Ocular Vestibular Evoked Myogenic Potential (cVEMP and oVEMP)

Intervention Type DIAGNOSTIC_TEST

Petrous bone Computed Tomography (CT)

For patients diagnosed with hearing loss, whether conductive, mixed, and/or a vestibular deficit, a CT scan (without injection) will be proposed for their care.

Petrous bone Computed Tomography (CT) is an imaging technique used as the standard method of evaluation of the boney structures in the ear.

Intervention Type DIAGNOSTIC_TEST

Magnetic Resonance Imaging (MRI)

Patients that have done a CT and for who CT results was abnormal, will additionally require an MRI for their standard care.

Magnetic Resonance Imaging (MRI) is an imaging technique used as the standard method of evaluation of the cochlear, retrocochlear and central and peripheral nervous system. An injection of Gadolinium contrast media will be used to enhance certain recordings.

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* 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 Criteria

* 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
* Ophthalmologic pathologies e.g. strabism or severe refraction disorder
* Patients under AME (State Medical Aid)
* Protected adult patients, adults unable to express their consent, pregnant or breastfeeding women
Minimum Eligible Age

12 Years

Maximum Eligible Age

20 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

URC-CIC Paris Descartes Necker Cochin

OTHER

Sponsor Role collaborator

Assistance Publique - Hôpitaux de Paris

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Natalie Loundon, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Assistance Publique - Hôpitaux de Paris

Marine Parodi, MD

Role: STUDY_DIRECTOR

Assistance Publique - Hôpitaux de Paris

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Hôpital Necker-Enfants Malades

Paris, , France

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

France

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Natalie Loundon, MD, PhD

Role: CONTACT

1 71 39 67 82 ext. +33

Hélène Morel

Role: CONTACT

1 71 19 63 46 ext. +33

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Natalie Loundon, MD, PhD

Role: primary

1 71 39 67 82 ext. +33

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

2022-A00375-38

Identifier Type: OTHER

Identifier Source: secondary_id

APHP220305

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Osteoporosis in RETT Syndrome
NCT02110797 COMPLETED NA
The BoDI (Bone Density Investigation) Study
NCT06117124 NOT_YET_RECRUITING NA
Resting-state Imaging and OSteoporosiS
NCT07030205 NOT_YET_RECRUITING NA