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

B

Buddhist Tzu Chi General Hospital

Status

Invitation-only

Conditions

Myopia
Anisometropia

Treatments

Device: Misight 1 Day Contact Lens

Study type

Observational

Funder types

Other

Identifiers

NCT06744478
IRB113-170-A

Details and patient eligibility

About

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.

Enrollment

50 estimated patients

Sex

All

Ages

8 to 23 years old

Volunteers

No Healthy Volunteers

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

Trial design

50 participants in 1 patient group

myopic children
Description:
Myopic children use Misight 1 Day Contact Lens every day for myopia and anisometropia control.
Treatment:
Device: Misight 1 Day Contact Lens

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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