A study to investigate the Efficacy, Safety, Acceptability of Essilor® Stellest® Spectacle Lenses along with the testing of Quality of Life implications in slowing down Myopia progression, in children and adolescents in India.
Not Applicable
- Conditions
- Health Condition 1: H521- Myopia
- Registration Number
- CTRI/2024/08/071994
- Lead Sponsor
- Essilor® India Private Limited
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Inclusion should be progressive myopia based on change in RE in the previous year
2. Information on progression of myopia prior to treatment should be available
3. All participants wearing Essilor® Stellest® Lenses
Exclusion Criteria
Not Applicable
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare with change in SER over 1 year prior to use of Stellest lenses and Change in cycloplegic autorefraction (SER) from baseline upto 12 monthsTimepoint: Up to 12 months
- Secondary Outcome Measures
Name Time Method ilTimepoint: Nil