Ignite Creation Date:
2024-06-16 @ 11:52 AM
Last Modification Date:
2024-10-26 @ 3:31 PM
Study NCT ID:
NCT06452524
Status:
COMPLETED
Last Update Posted:
2024-06-11
First Post:
2024-05-24
Brief Title:
Prematurity and Ophthalmological Changes
Sponsor:
Ankara City Hospital Bilkent
Organization:
Ankara City Hospital Bilkent
Study Overview
Official Title:
The Precondition of Retinopathy of Prematurity on Visual Acuity Refraction Biometric Values Retinal and Choroidal Thickness in School-Aged Children
Status:
COMPLETED
Status Verified Date:
2024-06
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Ophthalmological differences in school-aged children with and without a history of retinopathy of prematurity
Detailed 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
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 Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None