Otoferlin Patient Registry and Natural History Study

Recruiting now

Conditions studied: Otoferlin-related Auditory Synaptopathy, Hearing Impairment

In brief

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.

Key facts

Study ID

NCT05946057

Run by

Tobias Moser

People needed

100

Starts

2023-02-21

Expected to finish

2048-02-21

Last updated by the study team

2025-05-28

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• A molecular genetic diagnosis involving biallelic variants in otoferlin (OTOF) and audiometry

You may not qualify if…

• Patients with evidence of non-OTOF molecular genetic diagnoses

Where it is running

• University Medical Center Goettingen — Goettigen, Lower Saxony, Germany (enrolling)

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.