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A Clinical Comparison of Two Multifocal Toric Soft Contact Lenses

NCT06438601 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 36

Last updated 2025-08-11

Study results available
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Summary

This study aims to compare the short-term clinical performance of the two study contact lenses.

Conditions

Interventions

DEVICE

Lens A (omafilcon A)

15 minutes of daily wear.

DEVICE

Lens B (comfilcon A)

15 minutes of daily wear.

Sponsors & Collaborators

  • CooperVision, Inc.

    lead INDUSTRY

Principal Investigators

  • Carole Maldonado-Codina, PhD,MCOptom · Eurolens Research

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
35 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-04-24
Primary Completion
2024-08-15
Completion
2024-08-15
FDA Device
Yes

Countries

  • United Kingdom

Study Locations

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Entities

Diseases

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 NCT06438601 on ClinicalTrials.gov