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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