Clinical Trials Directory

Trials / Completed

CompletedNCT06170658

1 Week Crossover Dispensing 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
30 (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 a silicone hydrogel daily disposable investigational contact lenses to a hydrogel daily disposable commercially available contact lenses.

Detailed description

This is a prospective, bilateral, double masked (participant and investigator), randomized, cross-over dispensing study with 1 week wearing period in each arm by comparing visual acuity and subjective vision quality.

Conditions

Interventions

TypeNameDescription
DEVICETest Lenses (stenfilcon A)Daily disposable, silicone hydrogel investigational lenses for one week
DEVICEControl Lenses (omafilcon A)Daily disposable, hydrogel commercially available lenses for one week

Timeline

Start date
2023-12-11
Primary completion
2024-08-21
Completion
2024-08-21
First posted
2023-12-14
Last updated
2025-08-06

Locations

1 site across 1 country: Canada

Regulatory

Source: ClinicalTrials.gov record NCT06170658. Inclusion in this directory is not an endorsement.

1 Week Crossover Dispensing Study Between Two Soft Contact Lenses (NCT06170658) · Clinical Trials Directory