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Clinical Trials/NCT04689503
NCT04689503
Completed
Not Applicable

Study on the Measurement of Retinal Blood Flow in Children Based on Oct Angiography and the Effect of Optical Defocus Application

Wenzhou Medical University1 site in 1 country1,200 target enrollmentMay 1, 2017
ConditionsMyopia

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Myopia
Sponsor
Wenzhou Medical University
Enrollment
1200
Locations
1
Primary Endpoint
Blood flow density measurement
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

In order to provide reference for clinical application, the normal values of retinal blood flow parameters in Chinese healthy children were measured by oct-angiography. Meanwhile, the repeatability and consistency of retinal blood flow parameters measured by oct-angiography in children were further analyzed, and the correlation of retinal blood flow parameters with eye axis, choroidal thickness, age and diopter was analyzed, so as to provide basis for clinical diagnosis of children's ophthalmopathy. Objective to study the effect of short-term optical defocusing on retinal blood flow parameters, and analyze the correlation between the changes of posterior segment parameters before and after short-term optical defocusing, so as to provide the basis for the possible compensation mechanism of posterior segment optical defocusing, and further understand the possible physiological mechanism of myopia.

Registry
clinicaltrials.gov
Start Date
May 1, 2017
End Date
November 11, 2019
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Yune Zhao

vice-president

Wenzhou Medical University

Eligibility Criteria

Inclusion Criteria

  • The subjects should be 6-18 years old, with parents' consent and be able to abide by the experimental rules;
  • uncorrected visual acuity or spectacle corrected visual acuity ≥ 1.0, and each eye can fix the target;
  • equivalent spherical lens range + 0.50D \~ - 6.00D, binocular spherical lens anisometropia ≤ 1D, anisometropia ≤ 1.5D;
  • frame glasses can be worn for patients with ametropia, and hard contact lenses can not be worn for at least 4 weeks, and anisometropia can not be worn for 2 weeks
  • intraocular pressure in the normal range (9mmhg-21mmhg)

Exclusion Criteria

  • Patients with history of ocular trauma and surgery;
  • patients with ocular organic lesions or systemic diseases;
  • patients with dry eye;
  • patients in the treatment period using drugs (such as atropine eye drops);
  • patients with poor cooperation or unqualified image quality

Outcomes

Primary Outcomes

Blood flow density measurement

Time Frame: 2017.05.01-2019.11.11

The vascular density was defined as the percentage of the area occupied by the vascular cavity after secondary reconstruction. The percentage of vascular lumen in macular area is automatically displayed based on the early treatment of diabetic retinopathy study (ETDRS) partition (i.e. macular area, paramacular area, temporal area, last time area, nasal area and inferior area), and the other partition method is based on the "Nine Palace" partition (i.e. central macular area, supratemporal area, superior area, Supranasal area, nasal area, infranasal area, inferior area, infratemporal area and temporal area)

Secondary Outcomes

  • Macular avascular area measurement(2017.05.01-2019.11.11)

Study Sites (1)

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