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A Clinical Comparison of Two Soft Contact Lenses (C24-755)

NCT06758076 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 52

Last updated 2026-04-13

No results posted yet for this study

Summary

The aim of this study is to compare the short-term clinical performance of two soft contact lenses.

Conditions

  • Hyperopia
  • Myopia

Interventions

DEVICE

Lens 1 (ocufilcon D)

15 minutes of daily wear

DEVICE

Lens 2 (somofilcon A)

15 minutes of daily wear

Sponsors & Collaborators

  • CooperVision, Inc.

    lead INDUSTRY

Principal Investigators

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

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-11-18
Primary Completion
2025-01-31
Completion
2025-01-31
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 NCT06758076 on ClinicalTrials.gov