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

NCT01235624 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1161

Last updated 2013-11-06

No results posted yet for this study

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."

Conditions

  • Autosomal Dominant Retinitis Pigmentosa

Interventions

GENETIC

genetic analysis

Sponsors & Collaborators

  • Ministry of Health, France

    collaborator OTHER_GOV

  • University Hospital, Montpellier

    lead OTHER

Principal Investigators

  • christian HAMEL, Pr Ph.D · Institut National de la Santé Et de la Recherche Médicale, France

  • José-Alain SAHEL, Pr · § Centre hospitalier national d'ophtalmologie des XV-XX, Paris,FRANCE

  • Jean Louis DUFIER, Pr · Hopital Necker enfants-malades,Paris,FRANCE

  • Hélène DOLLFUS, Pr · CHU de STRASBOURG, FRANCE

  • sylvie ODENT, Pr · CHU de RENNES Unité INSERM 598,Paris,FRANCE

  • Sabine DEFOORT- DHELEMMES, Ph.D · CHRU de LILLE,FRANCE

  • Michel WEBER, Pr · CHU de NANTES,FRANCE

  • Xavier ZANLONGH, Ph.D · CLINIQUE SOURDILLE, NANTES,France

  • Laurence LO OLIVIER-FAIVRE, PH · Centre génétique Médicale - Children Hospital of DIJON

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
5 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2009-03-31
Primary Completion
2013-04-30
Completion
2013-04-30

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01235624 on ClinicalTrials.gov