The Effect of +3.00ADD on Myopia Progression in Chinese Children
Primary Purpose
Myopia
Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
two spectacles
single vision spectacles
Sponsored by
About this trial
This is an interventional prevention trial for Myopia focused on measuring +3.00ADD, single vision spectacle
Eligibility Criteria
Inclusion criteria
- Children who are aged 8 to 12 years (grade 3 and grade 4) from Huadu district of Guangzhou in China.
- Refractive error meeting all the following, obtained by cycloplegic autorefraction: spherical equivalent -1.00 to -6.00D in both eyes, astigmatism ≤2.00 D in both eyes, and spherical equivalent anisometropia ≤1.50 D.
- The best corrected visual acuity is ≥ 6/9.5
- The parents are willing to provide consent to participation in the study, and the children are willing to wear the only provided spectacles
Exclusion criteria
- Children who are allergy to tropicamide or topical anesthetic drugs.
- Children who had other eye diseases that cause the visual impairment including strabismus, amblyopia, ocular surface related disease, cataract, traumas, ocular fundus diseases, and ocular surgery.
- Children who were wearing rigid gas permeable contact lenses, progressive-addition lenses, bifocal spectacles lens, Peripheral defocus modifying contact lenses;
- Children who are receiving visual function training.
Sites / Locations
- Zhongshan Ophthalmic Center, Sun Yet-san UniversityRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
two spectacles
single vision spectacles
Arm Description
Outcomes
Primary Outcome Measures
spherical equivalent refraction (SER) change
SE was measured by autorefractometer with cycloplegic once a year at scheduled time
Secondary Outcome Measures
axial length
Axial length is measured by IOMaster once a year at scheduled time
corneal curvature
Corneal curvature is measured by IOMaster once a year at scheduled time
binocular vision
the binocular vision was measured by an ophthalmologist every six month at scheduled time.
Full Information
NCT ID
NCT03242226
First Posted
July 31, 2017
Last Updated
September 3, 2018
Sponsor
Zhongshan Ophthalmic Center, Sun Yat-sen University
1. Study Identification
Unique Protocol Identification Number
NCT03242226
Brief Title
The Effect of +3.00ADD on Myopia Progression in Chinese Children
Official Title
The Effect of +3.00ADD on Myopia Progression in Chinese Children: A Cluster Randomized Controlled Clinical Trial
Study Type
Interventional
2. Study Status
Record Verification Date
September 2018
Overall Recruitment Status
Unknown status
Study Start Date
October 11, 2016 (Actual)
Primary Completion Date
December 31, 2018 (Anticipated)
Study Completion Date
December 31, 2018 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Zhongshan Ophthalmic Center, Sun Yat-sen University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is to evaluate the effect of +3.00ADD vs single vision spectacle on the progression of myopia in children. Many studies applying bifocals or multifocal spectacles to intervene the progression have been carried out based on the idea that myopia was caused by excessive accommodation, however, the effect was limited. The possible reason is that bifocal or multifocal spectacles still not fully adjust the accommodative error in myopia children.
Detailed Description
The optical intervention has been extensively explored for the intervention of myopia progression.
Based on the theory that myopia was caused by the excessive accommodative, bifocal or multifocal spectacles for slowing the progression of myopia have been fully studied. Although some studies' results showed statistically significant for slowing myopia progression with multifocal spectacles, few had clinically meaningful, even in children with high accommodative lag or near-point esophoria. The investigators think that the possible reason for this clinical un-meaningful maybe that daily wearing bifocal or multifocal spectacles still not fully adjust the accommodative error in children.
The aim of this randomized clinical trial is to evaluate myopic progression in children using two spectacles (single-vision spectacles for distant vision, and +3.00ADD spectacle for near vision), compared with control subjects wearing one spectacles (single-vision spectacles). Myopia progression quantified by changes in axial length (AL) and cycloplegic spherical equivalent refraction will be monitored for 3 years. The spectacles for intervention group children will be adjusted based on the cycloplegic spherical equivalent and the extent of accommodation lag for schedule time.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Myopia
Keywords
+3.00ADD, single vision spectacle
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
440 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
two spectacles
Arm Type
Experimental
Arm Title
single vision spectacles
Arm Type
Active Comparator
Intervention Type
Device
Intervention Name(s)
two spectacles
Intervention Description
single-vision spectacles for distant vision, and +3.00ADD spectacle for near vision
Intervention Type
Device
Intervention Name(s)
single vision spectacles
Intervention Description
Wear single vision spectacle only
Primary Outcome Measure Information:
Title
spherical equivalent refraction (SER) change
Description
SE was measured by autorefractometer with cycloplegic once a year at scheduled time
Time Frame
3 years
Secondary Outcome Measure Information:
Title
axial length
Description
Axial length is measured by IOMaster once a year at scheduled time
Time Frame
3 years
Title
corneal curvature
Description
Corneal curvature is measured by IOMaster once a year at scheduled time
Time Frame
3 years
Title
binocular vision
Description
the binocular vision was measured by an ophthalmologist every six month at scheduled time.
Time Frame
3 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
8 Years
Maximum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria
Children who are aged 8 to 12 years (grade 3 and grade 4) from Huadu district of Guangzhou in China.
Refractive error meeting all the following, obtained by cycloplegic autorefraction: spherical equivalent -1.00 to -6.00D in both eyes, astigmatism ≤2.00 D in both eyes, and spherical equivalent anisometropia ≤1.50 D.
The best corrected visual acuity is ≥ 6/9.5
The parents are willing to provide consent to participation in the study, and the children are willing to wear the only provided spectacles
Exclusion criteria
Children who are allergy to tropicamide or topical anesthetic drugs.
Children who had other eye diseases that cause the visual impairment including strabismus, amblyopia, ocular surface related disease, cataract, traumas, ocular fundus diseases, and ocular surgery.
Children who were wearing rigid gas permeable contact lenses, progressive-addition lenses, bifocal spectacles lens, Peripheral defocus modifying contact lenses;
Children who are receiving visual function training.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yuting LI, Master
Phone
+86-020-87334687
Email
ytdorothy@163.com
First Name & Middle Initial & Last Name or Official Title & Degree
Qianyun Chen, Bachelor
Phone
+86-020-87334687
Email
torunchen@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yizhi LIU, MD,PhD
Organizational Affiliation
Zhongshan Ophthalmic Center, Sun Yat-sen University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Yangfa ZENG, MD,Master
Organizational Affiliation
Zhongshan Ophthalmic Center, Sun Yat-sen University
Official's Role
Study Director
Facility Information:
Facility Name
Zhongshan Ophthalmic Center, Sun Yet-san University
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510000
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yuting LI, Master
Phone
+86-020-87334687
Email
ytdorothy@163.com
First Name & Middle Initial & Last Name & Degree
Qianyun Chen, bachelor
Phone
+86-020-87334687
Email
torunchen@163.com
12. IPD Sharing Statement
Plan to Share IPD
Undecided
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The Effect of +3.00ADD on Myopia Progression in Chinese Children
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