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Clinical Assessment of Two Daily Wear Reusable Soft Silicone Hydrogel Contact Lenses

NCT05056987 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 36

Last updated 2023-06-18

Study results available
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Summary

The overall objective of this clinical study is to describe the clinical performance of the TOTAL30® soft contact lens compared to the ACUVUE® OASYS® with HYDRACLEAR PLUS (AOHP) soft contact lens in a daily wear modality.

Conditions

  • Refractive Errors

Interventions

DEVICE

Lehfilcon A contact lenses

CE-marked spherical soft contact lenses worn according to to the product package insert/Instructions for Use

DEVICE

Senofilcon A contact lenses

CE-marked spherical soft contact lenses worn according to to the product package insert/Instructions for Use

DEVICE

AOSEPT PLUS with HydraGlyde

Hydrogen peroxide-based cleaning and disinfecting solution

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Principal Investigators

  • Clinical Trial Lead, Vision Care · Alcon Research, LLC

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-01-12
Primary Completion
2022-06-14
Completion
2022-06-14
FDA Device
Yes

Countries

  • United Kingdom

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 NCT05056987 on ClinicalTrials.gov