NCT lookup

Pull any trial record directly from ClinicalTrials.gov.

Comparison of MiSight 1-Day and Acuvue Oasys for Presbyopia in Myopic Children
Comparison of MiSight 1-Day and Acuvue Oasys for Presbyopia in Myopic Children

NCT06887920

Active Not RecruitingNA

Sponsor: Pauline Kang

Conditions: Myopia Progressing

Interventions: Acuvue Oasys for Presbyopia, MiSight 1 Day

Countries: Australia

This study will compare the effects on myopia progression over the course of one year for eyes wearing MiSight 1 Day contact lenses compared to ACUVUE OASYS for PRESBYOPIA contact lenses.

Eligibility overview

Sex: ALL

Age: 6 Years to 12 Years

Healthy volunteers: No

Study type: INTERVENTIONAL

Eligibility criteria
Inclusion Criteria:

1. Aged 6-12 years (inclusive)
2. Is willing to wear soft contact lenses daily
3. Spherical equivalent myopic refractive error between -0.50 to -5.00 D in each eye and astigmatism \< 1.00 D
4. Best corrected logMAR visual acuity of 0.1 or better in both eyes
5. Good ocular and general health
6. No previous use of myopia control interventions for more than 1 month or within the last 30 days
7. Competent enough in English to be able to fully understand the participant information and consent form

Exclusion Criteria:

1. Strabismus at distance or near, amblyopia or significant anisometropia (\>1D)
2. Systemic or ocular conditions that may affect contact lens use (e.g., allergy) or that may affect refractive development (e.g., ptosis)
3. Previous history of ocular surgery, trauma, or chronic ocular disease
4. Contraindications to contact lens use
5. Ocular or systemic medication use which may interfere or interact with contact lens wear or ocular development
6. Plans to migrate or move during the study
7. Child, parents or guardians not willing to comply with treatment and/or follow-up schedule
Locations (1)
  • Sydney, New South Wales, Australia