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Phenotype Correlates Genotype of Inherited Retina Dystrophies, Retinitis Pigmentosa, Con>Rod Dystrophies.

NCT03990727 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 17000

Last updated 2019-06-19

No results posted yet for this study

Summary

Patients with retina dystrophies (retinitis pigmentosa, cone\>rods dystrophies, Usher and syndromic) will be correlated with genotype and validate inheritance mode by segregation analysis.

Conditions

Interventions

DIAGNOSTIC_TEST

Retina Analysis-mosaic

Fundus retina pattern study

DIAGNOSTIC_TEST

Autofluorescence

Fundus reflectance-functionality

DIAGNOSTIC_TEST

OCT- 1 micra

Fine tomography fundus retina

PROCEDURE

Genotype analysis

Molecular target retina dystrophy analysis

Sponsors & Collaborators

  • Maisonneuve-Rosemont Hospital

    collaborator OTHER

  • Retina and Genomics Institute

    collaborator UNKNOWN

  • MejoraVisionMD

    lead NETWORK

Eligibility

Min Age
2 Weeks
Max Age
90 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2009-08-31
Primary Completion
2019-06-13
Completion
2025-09-30

Countries

  • Mexico

Study Locations

More Related Trials

Entities

Diseases

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 NCT03990727 on ClinicalTrials.gov