Otoferlin Patient Registry and Natural History Study
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorTobias Moser
About this trial
This registry is designed to collect comprehensive information about the molecular genetic diagnoses of individuals with otoferlin-associated hearing impairment and clinical information to support a natural history study.
Eligibility criteria
Qualifiers
A molecular genetic diagnosis involving biallelic variants in otoferlin (OTOF) and audiometry
Disqualifiers
Patients with evidence of non-OTOF molecular genetic diagnoses
Trial design
Treatments tested in this trial
- Molecular genetic testing and audiometry
Treatment groups
100 Participants
are divided into 1 treatment groupLocations
1Map coordinates are unavailable for these locations. Locations are shown below instead.
University Medical Center GoettingenRecruiting37075, Goettigen, Lower Saxony
Germany
GermanySponsors and collaborators
Tobias Moser
Lead sponsor
University Medical Center Goettingen
Sponsor institution
Source ClinicalTrials.gov