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Clinical Trial Summary

Ophthalmological differences in school-aged children with and without a history of retinopathy of prematurity


Clinical Trial Description

Aims: To compare functional (visual acuity and refractive error) and anatomical (biometric values, foveal and choroidal thickness) ophthalmological differences in school-aged children with and without a history of retinopathy of prematurity (ROP). Settings and Design: Prospective Cross-Sectional Study Methods and Material: The study was conducted prospectively in the ophthalmology department of Ankara Bilkent City Hospital. Subjects were divided into three groups: 29 children who were treated with laser photocoagulation (ROP-TxGroup), 26 children who developed ROP and did not need treatment (ROP-non-TxGroup), and 25 children who did not develop ROP (Premature Group). The 27 healthy children with a history of full-term born (Control Group), who were in a similar age group for 'control eye examination', were accepted as the control group. A total of 107 patients and 211 eyes were included in the study. Non-cycloplegic and cycloplegic refraction, best corrected visual acuity (BCVA), keratometry, axial length (AL) and anterior chamber depth (ACD), optical coherence tomography (OCT) macular and OCT subfoveal choroidal measurements were performed in all cases. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06452524
Study type Observational [Patient Registry]
Source Ankara City Hospital Bilkent
Contact
Status Completed
Phase
Start date September 1, 2021
Completion date May 1, 2022

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