N/A
N=11
Audiovestibular Function in Infratentorial Superficial Siderosis
Siderosis · Neurological Disorder · Rare Diseases · Age Related Hearing Loss · Presbycusis
Bottom Line
View on ClinicalTrials.gov: NCT04200664 ↗Enrolled (actual)
11
Serious AEs
0.0%
Results posted
Jun 2025
Primary outcome: Primary: Hearing Evaluation - Pure Tone Audiometry — 57.3 decibel hearing level
Study Design & Population
- Study type
- Observational
- Phase
- N/A
- Interventions
- Hearing assessment (Diagnostic_test); Vestibular/balance assessment (Diagnostic_test); Quality of life assessment (Other); Olfactory (smell) function testing (Diagnostic_test); DNA bio-banking (Genetic)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- University College, London
- Primary completion
- Oct 2021
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Hearing Evaluation - Pure Tone Audiometry |
57.3 | — |
| PRIMARY Vestibular/Balance Evaluation |
6; 1; 3; 9; 1; 0 | — |
| PRIMARY Hearing Evaluation - Auditory Brainstem Responses/Acoustic Reflexes |
5; 2; 4 | — |
| PRIMARY Hearing Evaluation - Tympanogram |
0; 11 | — |
| PRIMARY Hearing Evaluation - Otoacoustic Emissions |
3; 3; 5 | — |
| PRIMARY Hearing Evaluation - Listening in Spatialised Sentences Noise Test |
4; 1; 6 | — |
| SECONDARY Correlation Between Clinically Obtained Imaging (Siderosis Group Participants) and the Hearing and Balance Assessment Results |
10; 0; 10; 0; 10; 0 | — |
| SECONDARY Correlation Between Clinically Obtained Results of Cognitive Function Assessment (Siderosis Group Participants) and the Hearing and Balance Assessments |
7; 5; 5 | 0.176 |
| SECONDARY Smell Identification Test |
25.5 | — |
Summary
One in six people in the United Kingdom and over 400 million people worldwide have disabling hearing loss. This figure will double by 2050 as predicted by the World Health Organisation. There is an urgent need to improve our knowledge regarding hearing loss, its underlying mechanisms, optimal diagnostic modalities, reliable and accurate functional and imaging biomarkers.
A less-well studied condition associated with progressive hearing loss is infratentorial superficial siderosis (iSS). It results from iron deposition along the surfaces of brain structures which control hearing and balance. It is currently considered uncommon, but may well be under-recognised and therefore under-reported. Despite its severity, our current understanding of its impact on the hearing (auditory) and balance (vestibular) functions is limited, and this has an adverse impact on the treatment offered to these patients. Additionally, iSS patients have been reported to have cognitive impairment yet literature reports of cognitive assessment in iSS are few. The cognitive dysfunction may be specific to iSS or due to progressive hearing impairment or a combination of both, and further studies are required to establish this. Olfaction is also known to be affected in patients with iSS yet is rarely reported in the literature.
Due to the significant morbidity and progressive nature, there is a clear need to improve our understanding of the audiovestibular dysfunction resulting from iSS.
The aim of this study is to comprehensively assess audiovestibular function in iSS compared to age-related hearing loss and the controls/normative data and as a means to quantify deficits for monitoring disease progression and response to treatment, to assess the impact on the quality of life, to analyse clinically-obtained data (including imaging, cognitive and laboratory data), and correlate these with functional findings in iSS.
Eligibility Criteria
Inclusion Criteria
- Siderosis group: adults (male and female) of 18+ years old with a known diagnosis of iSS (defined using standardised radiological criteria) confirmed by a consultant neurologist with expertise in this condition at University College London Hospitals National Health Service (NHS) Foundation Trust
- Age-related hearing loss (ARHL) group: adults (male and female) of 18+ years old with ARHL
- Control group: adults (male and female) of 18+ years old with no previous diagnosis of hearing loss or no known neurological disorder (including iSS) that affects hearing, with the aim to recruit such participants of 50 years of age and above; however, should difficulty with the recruitment of such participants arise, participants of 18 years of age and above will be invited to participate in the study.
Exclusion Criteria
- All groups: individuals younger than 18 years old; individuals with a physical or mental impairment that prevents the potential participant from giving informed consent or undergoing the hearing and/or vestibular assessment;
- Siderosis group: individuals with no prior diagnosis of iSS
- Age-related hearing loss (ARHL) group: individuals with no previous diagnosis of ARHL or with a diagnosis of hearing loss of aetiology other than age-related; individuals with a history of exposure to high-intensity noise or ototoxic drugs or evidence of middle ear disease/dysfunction or family history of non age-related hearing loss;
- Control group: individuals with a known history of hearing loss (of any cause) or with a known neurological disorder that affects their hearing; individuals with history of exposure to high-intensity noise or ototoxic drugs or evidence of middle ear disease or family history of non age-related hearing loss;
Data sourced from ClinicalTrials.gov (NCT04200664). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.