Clinical Trials Directory

Trials / Completed

CompletedNCT06611410

1 Week Crossover Study Between Two Soft Contact Lenses

1 Week Crossover Dispensing Study: Buttermere Versus MiSight 1 Day Soft Contact Lenses

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
10 (actual)
Sponsor
CooperVision, Inc. · Industry
Sex
All
Age
8 Years – 18 Years
Healthy volunteers
Not accepted

Summary

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

Detailed description

This is a prospective, multiple day, double (investigator and subject) masked, randomized, bilateral crossover study comparing a Test lens against an appropriate Control lens. Main aim is to compare visual acuity and subjective vision ratings of vision quality between two lenses in habitual soft lens wearers.

Conditions

Interventions

TypeNameDescription
DEVICETest Lenses (stenfilcon A)Daily disposable, soft contact lenses worn for one week.
DEVICEControl Lenses (omafilcon A)Daily disposable, soft contact lenses worn for one week.

Timeline

Start date
2024-06-05
Primary completion
2024-07-26
Completion
2024-07-26
First posted
2024-09-25
Last updated
2025-10-15
Results posted
2025-10-15

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT06611410. Inclusion in this directory is not an endorsement.

1 Week Crossover Study Between Two Soft Contact Lenses (NCT06611410) · Clinical Trials Directory