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Assessing the Magnitude of Anisometropia in Patients Wearing Misight 1 Day Contact Lens

Conditions
Myopia
Anisometropia
Registration Number
NCT06744478
Lead Sponsor
Buddhist Tzu Chi General Hospital
Brief Summary

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.

Detailed Description

Not available

Recruitment & Eligibility

Status
ENROLLING_BY_INVITATION
Sex
All
Target Recruitment
50
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

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Changes of the visual acuity in myopic children with different Misight 1 Day Contact LensFrom the date of starting treatment, the visual acuity was measured 1 week, 1month and every 3 months up to 24 months.

The investigators measure the visual acuity of myopic children with different Misight 1 Day Contact Lens.

Secondary Outcome Measures
NameTimeMethod
Changes of axial length in myopic children with different Misight 1 Day Contact LensFrom the date of starting treatment, the axial length was measured, then repeat measure were performed every 6 months up to 24 months

The investigators measure the axial length(mm) of eyeball of myopic children with different diopter of Misight 1 Day Contact Lens.

Trial Locations

Locations (1)

Shang-Yen WU

🇨🇳

Hualien City, Taiwan

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