Natural History Study of Usher Syndrome ( Light4Deaf ) | ClinicalTrials HQ

Ask about research services

Swipe the table sideways for more columns.

Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Natural History Study of Usher Syndrome ( Light4Deaf )	Abnormalities, Multiple, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Deaf-Blind Disorders, Deafness, Ear Diseases, Eye Diseases, Hereditary, Hearing Loss, Sensorineural, Neurologic Manifestations, Pathological Conditions, Signs and Symptoms, Sensation Disorders, Signs and Symptoms, Usher syndrome, blindness (disorder), eye disorder, hearing disorder, hearing loss disorder, hereditary disease, inherited retinal dystrophy, nervous system disorder, otorhinolaryngologic disease, retinal degeneration, retinal disorder, retinitis pigmentosa, vision disorder	Recruiting	Not stated	2020-12-14		NCT04665726

2 results · Page 1 of 1

Swipe the table sideways for more columns.

Organizations	Linked trials
Assistance Publique - Hôpitaux de Paris	985
Centre Hospitalier National d'Ophtalmologie des Quinze-Vingts	15

4 results · Page 1 of 1

Swipe the table sideways for more columns.

Research sites	City	Country	Linked trials
Centre Hospitalier National d'Ophtalmologie des Quinze-Vingts	Paris	France	6
CHU Necker	Paris	France	1
CHU Pitié Salpêtrière	Paris	France	2
CHU Robert Debré	Paris	France	2