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NCT07514039

Photolithography Microstructure Myopia Management Lenses in Preventing and Controlling Myopia in Children and Adolescents

ENROLLING BY INVITATION NA Last updated 7 April 2026
What this trial tests

NA trial testing Myopia management lens in Myopia, Child Myopia Progression in 252 participants. Enrolling by invitation.

Timeline
1 February 2026
Primary endpoint
30 August 2027
31 December 2027

Quick facts

Lead sponsorShanghai Eye Disease Prevention and Treatment Center
PhaseNA
StatusENROLLING BY INVITATION
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingtriple
Primary purposeprevention
Enrollment252
Start date1 February 2026
Primary completion30 August 2027
Estimated completion31 December 2027
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Shanghai Eye Disease Prevention and Treatment Center — full company profile →

Who can join

Adults 6 to 14, any sex, with Myopia, Child Myopia Progression. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Evaluate the effectiveness of different lithographic microstructured myopia management lenses in controlling the progression of myopia in children and adolescents, as well as the safety and comfort of wearing them. Explore effective defocus microlens designs for myopia control and the feasibility of applying lithographic microstructured myopia management lenses in myopia prevention and control.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Myopia, Child Myopia Progression

Currently open trials in the same condition.

Other Shanghai Eye Disease Prevention and Treatment Center trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07514039.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing