Status
Conditions
Treatments
About
The study is aimed to observe the short-term clinical performance of MiSight™ multifocal soft contact lens compared with Proclear™ 1day, including objective examination, subjective acceptability of wearers, and doctors' evaluation of the clinical manifestations of lenses.
Full description
Compared with Proclear™ 1day, observe the short-term clinical performance of MiSight™ multifocal soft contact lens including objective examination, subjective acceptability of wearers, and doctors' evaluation of the clinical manifestations of lenses in 1 month.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
• Prior to being considered eligible to participate in this study, each subject MUST:
Be between 8 and 12 years of age inclusive at the baseline examination.
Have:
Have their parent or legal guardian:
Along with their parent or guardian, be capable of comprehending the nature of the study and be willing and able to adhere to the instructions set forth in this protocol.
Along with their parent or guardian, agree to maintain the visit schedule and be able to keep all appointments as specified in the study protocol for the duration of the study.
Agree to wear the assigned contact lenses for the duration of the 1-month study and to inform the study investigator if this schedule is interrupted. (Wearing time may be modified by the study staff for health reasons.)
Meet the following refractive criteria determined by cycloplegic autorefraction at baseline:
Best-corrected visual acuity :≥0.8.
Exclusion criteria
• Subjects may not be considered eligible if ANY of the following apply:
Primary purpose
Allocation
Interventional model
Masking
40 participants in 1 patient group
Loading...
Data sourced from clinicaltrials.gov
Clinical trials
Research sites
Resources
Legal