Status:

COMPLETED

TGFB1 And LAMA1 Gene Polymorphisms in High Myopia

Lead Sponsor:

Ege University

Conditions:

High Myopia

Gene Mutations

Eligibility:

All Genders

3-13 years

Phase:

NA

Brief Summary

The investigators aimed to investigate TGFB1 and LAMA1 gene polymorphisms in children with high myopia in order to determine the genetic basis of large myopic shifts causing severe visual impairment a...

Eligibility Criteria

Inclusion

  • Patients under the age of 13
  • Patients with cycloplegic refraction values ≥6 D (for study group)
  • Emmetropic patients (for control group)

Exclusion

  • Patients who had additional ocular pathology that may affect refraction (such as glaucoma, cataracts, corneal disease)
  • Patients with history of ocular surgery

Key Trial Info

Start Date :

December 1 2012

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

June 1 2017

Estimated Enrollment :

151 Patients enrolled

Trial Details

Trial ID

NCT03451877

Start Date

December 1 2012

End Date

June 1 2017

Last Update

March 5 2018

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TGFB1 And LAMA1 Gene Polymorphisms in High Myopia | DecenTrialz