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Familial Analysis of Keratoconus Risk

NCT02812563 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 95

Last updated 2017-11-13

No results posted yet for this study

Summary

The principal objective of this study is to evaluate the frequency of KC inside family of patients with confirmed KC.

It's a familial, epidemiological, prospective, single-center study.

Conditions

  • Keratoconus

Interventions

OTHER

genetic

Galilee exam - Corn analysis with Optiwave Refractive Analysis

Sponsors & Collaborators

  • University Hospital, Bordeaux

    lead OTHER

Principal Investigators

  • David Touboul, MD · University Hospital Bordeaux, France

Eligibility

Min Age
7 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2014-11-25
Primary Completion
2017-09-19
Completion
2017-09-19

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 NCT02812563 on ClinicalTrials.gov