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Clinical Trials in China / NCT03666052
Enrolling by invitation Observational

Shanghai Child and Adolescent Large-scale Eye Study -High Myopia Registration

NCT03666052 · tracked via the Priya Life Science China tracker
Sponsor
Shanghai Eye Disease Prevention and Treatment Center
Phase
Observational
Started
2018-09-16
Last updated
2018-09-18

Condition(s) studied

High MyopiaPathologic Myopia

Study summary

1.1 Research objectives A.To observe the fundus changes in the posterior pole (morphology, thickness, asymmetry, blood flow density, etc) with the myopia progression.

B.To observe morphological changes in choroid and peripheral region of retina with myopia progression.

C. To observe changes of visual function (contrast sensitivity, Microperimetry, etc) with myopia progression.

D. To detect the susceptibility genes related to high myopia and myopic fundus changes; to test the levels of Vitamin D, riboflavin, transforming growth factor(TGF), insulin-like growth factor(IGF), fibroblast growth factor(FGF), etc.

E. To observe the changes of living quality, psychology, behavior and social activities of high myopic children.

1.2 Research design Prospective cohort study. After completing the baseline survey, the planned follow-up frequency is once a year.

1.3 Research cycle 2018.06\~2038.06 (at least).

1.4 Expected results A. Registration completed a study of high myopia research for children and adolescents covering around 3,000 people; B. Establish a database information management system and workflow SOP(standard operating procedure)file for the study of high myopia registration in children and adolescents; C. Further clarify the changes in the retinal, choroidal and scleral tissue structures, blood flow density, etc. in the macular area and the optic disc; D. Revealing the changes of the retina, choroid and other tissues in the peripheral area with the progression of myopia; E. To clarify the relationship between changes in the fundus structure and changes in visual function in the posterior pole; F. Further clarify the etiology and pathogenesis of high myopia, pathological myopia and myopic fundus lesions, and identify the relationship between high myopia and pathological myopia; G. From the perspectives of society, behavior and psychology, the effects of high myopia and pathological myopia on children and adolescents will be fully demonstrated.

2\. Research object 2.1 General characteristics of the research object

Based on the refraction development archive system that has been constructed in Shanghai, the list of children and adolescents with high myopia was selected from the database of children's refractive development archives information in Shanghai. Children of different ages with high myopia must meet the following conditions:

1. 4-5 years old, equivalent spherical error(SE) ≤ -4.0 diopter(D);
2. 6-8 years old, equivalent spherical error(SE) ≤ -6.0 diopter(D);
3. 9-18 years old, equivalent spherical error(SE) ≤ -8.0 diopter(D).

2.2 Sample size A total of 1.25 million children and adolescents are currently registered, 4,006 (0.32%) of which meet the entry requirements. Among the 4\~5 year olds, there are 815 people with SE≤-4D; 842 people with SE≤-6 D among the 6\~8 year olds; 2349 people with SE≤-8D among the people aged 9 and over . Taking into account the 50% non-response and the proportion of the exclusion, the initial registration number is about 2,000.

2.3 Source of study object Children and adolescents who meet the inclusion criteria in the Shanghai Children's Refractive Development Archives Information Database System.

Eligibility

Sex
ALL
Min age
4 Years
Max age
18 Years
Healthy volunteers
No
Inclusion Criteria: * Children and adolescents between the ages of 4 and 18 years old, SE ≤ -4 D under 5 years old, SE ≤ -6 D at 6-8 years old, SE ≤ -8 D over 9 years old; * No eye disease, good general condition, can cooperate with the examiner; * Obtaining the consent of the child and his/her guardian; * Long-term residence in this city, there is no plan to move out of this city in the short term. Exclusion Criteria: * Amblyopia (best corrected visual acuity (BCVA) less than 0.8 for children over 6 years old, BCVA less than 0.63 for children 6 years old and younger) and strabismus; * Secondary myopia, genetic disease or connective tissue-related myopia; * Moderate or severe ptosis; * Congenital cataract, glaucoma; * Other fundus diseases other than myopic related fundus lesions; * Intraocular or refractive surgery history; * The refractive medium is turbid, and it is impossible to take a clear fundus image; * Unable to cooperate with fundus image shooting and other examination; * Do not receive cycloplegia or have contraindications; * Poor overall condition, unable to follow up for a long time; * The child or the guardian refuses to participate in the research; * Other cases in which the researcher judges that it is not suitable for participation in the study.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Shanghai Eye Disease Prevention & Treatment Center Shanghai Shanghai Municipality

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT03666052 on ClinicalTrials.gov ↗ ← All trials in China