Enrolling by invitation NCT06744478
Assessing the Magnitude of Anisometropia in Patients Wearing Misight 1 Day Contact Lens
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Misight 1 Day Contact Lens.
- Who it may be relevant to
- Registry conditions: Myopia, Anisometropia. Basic parameters: 8 years — 23 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Taiwan
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
The effectiveness of Misight 1 Day Contact Lens in retarding anisometropic progression has not been investigated before. This study is aimed to elucidate the efficacy of Misight 1 Day Contact Lens for anisometropia control.
Interventions
- Device Misight 1 Day Contact Lens
Misight 1 Day Contact Lens wearing for myopia control
Primary outcome measures
- Changes of the visual acuity in myopic children with different Misight 1 Day Contact Lens [Time frame: From the date of starting treatment, the visual acuity was measured 1 week, 1month and every 3 months up to 24 months.]
Secondary outcome measures (1)
- Changes of axial length in myopic children with different Misight 1 Day Contact Lens [Time frame: From the date of starting treatment, the axial length was measured, then repeat measure were performed every 6 months up to 24 months]
Eligibility criteria
Inclusion criteria
- 8-23 years old children diagnosed with anisometropia and are willing to accept MiSight® 1 Day contact lens wearing treatment.
- No congenital eye diseases or eye diseases such as strabismus and amblyopia.
- Those who have been stated to be willing to participate in the program for at least 24 months and accept various evaluations.
Exclusion criteria
- Ocular surface disease( dry eye, keratoconus..)
- Allergy to contact lens
- Received eye surgery before
- The cornea is infected (bacterial, fungal or viral infection).
- Strabismus
- Premature birth
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Study design
- Observational model
- Case-control
Study locations
Taiwan · 1 center
- Shang-Yen WU — Hualien City
Identifiers
NCT: NCT06744478 · IRB113-170-A