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1 Week Crossover Study Between Two Soft Contact Lenses

NCT06611410 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 10

Last updated 2025-10-15

Study results available
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Summary

The objective of this investigation is to compare the visual clinical performance of two daily disposable soft contact lenses.

Conditions

  • Myopia

Interventions

DEVICE

Test Lenses (stenfilcon A)

Daily disposable, soft contact lenses worn for one week.

DEVICE

Control Lenses (omafilcon A)

Daily disposable, soft contact lenses worn for one week.

Sponsors & Collaborators

  • CooperVision, Inc.

    lead INDUSTRY

Principal Investigators

  • Pete S Kollbaum, OD, PhD · Indiana University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
CROSSOVER

Eligibility

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

Timeline & Regulatory

Start
2024-06-05
Primary Completion
2024-07-26
Completion
2024-07-26
FDA Device
Yes

Countries

  • United States

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 NCT06611410 on ClinicalTrials.gov