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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT00627874
Other study ID # PLS2008
Secondary ID
Status Not yet recruiting
Phase N/A
First received February 20, 2008
Last updated February 20, 2009
Start date April 2010
Est. completion date April 2012

Study information

Verified date February 2009
Source Sun Yat-sen University
Contact n/a
Is FDA regulated No
Health authority China: Ethics Committee
Study type Interventional

Clinical Trial Summary

The purpose of this study is to assess whether a short-term imposed myopic defocus is effective in preventing the development and progression of juvenile-onset myopia in Chinese children.


Description:

1. To determine if +3D lenses wearing for half an hour everyday prevents the development and progression of myopia in school children.

2. To identify ocular parameters and risk factors at baseline associated with development and progression of myopia.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 1200
Est. completion date April 2012
Est. primary completion date April 2012
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- All children in the selected class are enrolled

Exclusion Criteria:

- Hyperopia > +2.0 D

- High myopia > -6.0 D

- Astigmatism> 1.5 D

- Anisometropia > 1.5 D

- Strabismus and amblyopia

- Any ocular, systemic, or neurodevelopmental conditions that could influence refractive development

- Chronic medication use that might affect myopia progression or visual acuity

- Already receiving other treatment for progressing myopia

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Device:
+3D Lenses
wear +3D glasses for 30 minutes per day and engage in activities which require vision at more than 1m

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Sun Yat-sen University Australian National University

Outcome

Type Measure Description Time frame Safety issue
Primary Axial Length of eyes Annual No
Secondary Autorefraction Annual No
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