Study on the Measurement of Retinal Blood Flow in Children
NCT ID: NCT04689503
Last Updated: 2020-12-30
Study Results
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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COMPLETED
1200 participants
OBSERVATIONAL
2017-05-01
2019-11-11
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
2. uncorrected visual acuity or spectacle corrected visual acuity ≥ 1.0, and each eye can fix the target;
3. equivalent spherical lens range + 0.50D \~ - 6.00D, binocular spherical lens anisometropia ≤ 1D, anisometropia ≤ 1.5D;
4. 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
5. intraocular pressure in the normal range (9mmhg-21mmhg)
Exclusion Criteria
2. patients with ocular organic lesions or systemic diseases;
3. patients with dry eye;
4. patients in the treatment period using drugs (such as atropine eye drops);
5. patients with poor cooperation or unqualified image quality
6 Years
18 Years
ALL
No
Sponsors
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Wenzhou Medical University
OTHER
Responsible Party
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Yune Zhao
vice-president
Locations
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The affiliated Eye Hospital of Wenzhou Medical College
Wenzhou, Zhejiang, China
Countries
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Other Identifiers
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retinal blood flow in children
Identifier Type: -
Identifier Source: org_study_id