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Short-term Clinical Performance of Multifocal Soft Contact Lens

NCT05273606 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2022-12-28

No results posted yet for this study

Summary

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.

Conditions

  • Myopia

Interventions

DEVICE

MiSight mutifocal soft contact lens

Subjects will wear MiSight™ multifocal soft contact lenses for 1 month.

DEVICE

Proclear 1 Day soft contact lens

Proclear™ 1 Day soft contact lens will be worn for baseline evaluation.

Sponsors & Collaborators

  • Zhongshan Ophthalmic Center, Sun Yat-sen University

    lead OTHER

Principal Investigators

  • Xiao Yang, PhD · Zhongshan Ophthalmic Center, Sun Yat-sen University

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
8 Years
Max Age
12 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-07-16
Primary Completion
2022-12-13
Completion
2022-12-16

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05273606 on ClinicalTrials.gov