Effects of Birth Weight on Anterior Eye Segment Measurements in Full-Term Children by Galilei Dual-Scheimpflug Analyzer

NCT ID: NCT02466932

Last Updated: 2015-06-09

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

78 participants

Study Classification

OBSERVATIONAL

Study Start Date

2011-01-31

Study Completion Date

2013-03-31

Brief Summary

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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.

Detailed Description

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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.

Conditions

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Birth Weight

Study Design

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Study Time Perspective

CROSS_SECTIONAL

Study Groups

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Birth Weight

Galilei Dual-Scheimpflug Analyzer

Intervention Type DEVICE

Measuring of Anterior Segment by Galilei Dual-Scheimpflug Analyzer

Interventions

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Galilei Dual-Scheimpflug Analyzer

Measuring of Anterior Segment by Galilei Dual-Scheimpflug Analyzer

Intervention Type DEVICE

Eligibility Criteria

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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.
Minimum Eligible Age

30 Months

Maximum Eligible Age

80 Months

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Ondokuz Mayıs University

OTHER

Sponsor Role collaborator

Neon Hospital

OTHER

Sponsor Role lead

Responsible Party

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Volkan YETER

Dr.

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

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2010-171

Identifier Type: -

Identifier Source: org_study_id

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