Effects of Birth Weight on Anterior Eye Segment Measurements in Full-Term Children by Galilei Dual-Scheimpflug Analyzer
Overview
This study evaluates the effects of birth weight (BW) on ocular anterior segment parameters in preschool children using the Galilei Dual-Sheimpflug Analyzer (GD-SA). Children were measured by GD-SA and relationships between all anterior segment parameters obtained by this device and birth weight were analyzed.
Study Type
- Study Type: Observational [Patient Registry]
- Study Design
- Time Perspective: Cross-Sectional
- Study Primary Completion Date: March 2013
Detailed Description
Preschoolers, who were born heavier, had thicker cornea and lens, longer axial length, and flatter corneal curve. The thicknesses and axial curves of central cornea within 7mm may be particularly associated with BW.
Interventions
- Device: Galilei Dual-Scheimpflug Analyzer
- Measuring of Anterior Segment by Galilei Dual-Scheimpflug Analyzer
Arms, Groups and Cohorts
- Birth Weight
Clinical Trial Outcome Measures
Primary Measures
- Measurements of anterior segment parameters in Full-Term Children by Galilei Dual-Scheimpflug Analyzer
- Time Frame: 1 day
- Corneal parameters, anterior chamber parameters and lens thickness were measured by Galilei Dual-Scheimpflug Analyzer in healthy preschool children.
Participating in This Clinical Trial
Inclusion Criteria
- ages 3- 6 years; – birth weight >2,500 g; – gestational age (i.e., the period of time between the first day of the mother's last menstrual period and birth) >37 weeks; – visual acuity >0.8 (in decimals); – no history of any systemic or ocular diseases; – no history of previous ocular surgeries; – no retinopathy of prematurity; – no current medications; and – no retinal or optic disc abnormalities on fundoscopy. Exclusion Criteria:
- ages <3 >6 years; – birth weight <2,500 g; – gestational age (i.e., the period of time between the first day of the mother's last menstrual period and birth) <37 weeks; – visual acuity <0.8 (in decimals); – history of any systemic or ocular diseases; – history of previous ocular surgeries; – retinopathy of prematurity; – current medications; and – retinal or optic disc abnormalities on fundoscopy.
Gender Eligibility: All
Minimum Age: 30 Months
Maximum Age: 80 Months
Are Healthy Volunteers Accepted: Accepts Healthy Volunteers
Investigator Details
- Lead Sponsor
- Neon Hospital
- Collaborator
- Ondokuz Mayıs University
- Provider of Information About this Clinical Study
- Principal Investigator: Volkan YETER, Dr. – Neon Hospital
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