To Evaluate the Efficacy and Safety of an Defocus Lens in Slowing the Progression of Myopia

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age8-13
SponsorTianjin Eye Hospital

About this trial

To confirm the efficacy of DIMS lenses in controlling myopia progression, we planned a prospective, single-centre, randomised, double-blind, controlled, non-inferiority clinical study.

Eligibility criteria

Qualifiers

The subjects had spherical RE of -1.00 to -6.00 D, astigmatism ≤ 1.50 D, anisometropia ≤ 1.50 D

the best corrected visual acuity in the left and right eyes subjective optometry is greater than or equal to 1.0

Disqualifiers

Candidate subjects were excluded from the study if they had strabismus, ocular limitations, or systemic abnormalities affecting vision and ocular motility

Trial design

Treatments tested in this trial

  • frame lens

Treatment groups

138 Participants
are divided into 3 treatment groups

Sponsors and collaborators