CompletedNot Applicable

Autosomal Dominant Retinitis Pigmentosa: Prevalence of Known Genes Identification of New Loci / Genes

France1,161 participantsStarted 2009-03

Plain-language summary

Identify new genes responsible for autosomal dominant retinitis pigmentosa (ADRP), one of the most common causes of hereditary diseases of the retina, and thus better understand the mechanisms involved of the disease."

Who can participate

Age range5 Years – 80 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * retinitis pigmentosa diagnosed * Autosomal dominant transmission diagnosed * Aged from 5 to 80 years * Informed consent * Affiliated or benefit from an insurance regimen Exclusion Criteria: \-

What they're measuring

identification of unknown loci and genes responsible of Autosomal dominant retinitis pigmentosa (adRP)

Timeframe: for 5 years

Trial details

NCT IDNCT01235624

SponsorUniversity Hospital, Montpellier

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2013-04

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