Status:

COMPLETED

Ophthalmological Abnormalities in Hereditary Ichthyosis (ICHTYO-KERATO)

Lead Sponsor:

University Hospital, Toulouse

Collaborating Sponsors:

Association for the development of research in Dermatology

Conditions:

Ichthyosis

Eligibility:

All Genders

6+ years

Phase:

NA

Brief Summary

Presence/absence of subclinical keratoconus with corneal topographic abnormalities (skewed radial axes for forme fruste keratoconus, and inferior steepening for keratoconus suspect) on axial specular ...

Detailed Description

Background: Hereditary ichthyosis are rare genetic diseases characterized by an abnormal epithelial keratinization due to mutations in gene involved in skin barrier. Patients present with scales on th...

Eligibility Criteria

Inclusion

  • For ichthyosis population:
  • Hereditary ichthyosis, whatever form or ongoing therapy.
  • Parental permission for minors
  • For controls:
  • Patients who consult an ophthalmologist for refractive surgery screening or systematic eye examination
  • Parental permission for minors

Exclusion

  • For both populations:
  • Patient who cannot stay seated
  • Wearing contact lens within the last 7 days
  • No social security
  • Past medical history of corneal or eye surgery or eye condition (glaucoma, uveitis, keratoconus, retinal diseases)
  • Impossibility to fill the questionnaires

Key Trial Info

Start Date :

July 18 2017

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

June 30 2022

Estimated Enrollment :

152 Patients enrolled

Trial Details

Trial ID

NCT03464994

Start Date

July 18 2017

End Date

June 30 2022

Last Update

December 31 2025

Active Locations (1)

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Page 1 of 1 (1 locations)

1

University Hospital of Toulouse

Toulouse, France, 31000

Ophthalmological Abnormalities in Hereditary Ichthyosis (ICHTYO-KERATO) | DecenTrialz