RecruitingNCT05402813

Natural History in Children up to 16 Years With Mild to Profound Hearing Loss Due to Mutations in GJB2 / OTOF Genes

Studying Holt-Oram syndrome

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Key facts

Sponsor
Sensorion
Principal Investigator
Natalie LOUNDON, MD
Necker Hospital
Intervention
Pure Tone Audiometry Assessment(other)
Enrollment
180 target
Eligibility
16 years · All sexes
Timeline
20222028

Study locations (1)

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT05402813 on ClinicalTrials.gov

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