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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00477620
Other study ID # FR-2005-01-01
Secondary ID
Status Completed
Phase N/A
First received May 23, 2007
Last updated February 19, 2009
Start date April 2004
Est. completion date October 2008

Study information

Verified date February 2009
Source University Hospital Freiburg
Contact n/a
Is FDA regulated No
Health authority Switzerland: Ethikkommission
Study type Interventional

Clinical Trial Summary

Purpose:

To determine whether the use of reading glasses blocks the near work mediated increased incidence of myopia in healthy school children.

Methods:

SMART enrolled 115 emmetropic children (ages 7-9 years). The children were recruited in the Principality of Liechtenstein. They were randomly assigned to either the control group (n=52) or to receive reading glasses with a lens power of +2.0 dioptres (n=63). The primary outcome measure was progression towards myopia as determined by autorefraction after cycloplegia. The secondary outcome measure was change in biometry measurements of corneal curvature, axial length, anterior chamber depth, crystalline lens thickness, and vitreous chamber depth using partial coherence interferometry.


Recruitment information / eligibility

Status Completed
Enrollment 0
Est. completion date October 2008
Est. primary completion date October 2008
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 7 Years to 9 Years
Eligibility Inclusion Criteria:

- Emmetropia

Exclusion Criteria:

- Ametropia

Study Design

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


Related Conditions & MeSH terms


Intervention

Behavioral:
Wearing of reading glasses during prolonged near work


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University Hospital Freiburg
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