Evaluation of Comfort in Symptomatic Contact Lens Wearers

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT04963543

Enrollment

Registered

2021-07-15

Start date

2021-07-22

Completion date

2021-10-29

Last updated

2021-11-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ocular Comfort

Keywords

Contact Lenses

Brief summary

The purpose of this study is to evaluate the comfort of an ocular lubricant in symptomatic contact lens wearers. This study will be conducted in Canada.

Detailed description

The duration of individual participation is six days.

Interventions

OTHERFID123238

Lubricant applied to the ocular surface

Study design

Allocation

Intervention model

SINGLE_GROUP

Primary purpose

OTHER

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

Key Inclusion Criteria: * Is able to understand and sign an approved information consent letter; * Habitually wears daily disposable soft contact lenses in both eyes; * Is able to achieve 20/40 or better monocular VA with habitual contact lenses; * Has a pair of spectacles for vision correction. * Other protocol-defined inclusion criteria may apply. Key

Exclusion criteria

* Routinely sleeps in habitual contact lenses; * Has any known active ocular disease and/or infection; * Is pregnant or lactating; * Other protocol-defined

Design outcomes

Primary

Measure	Time frame	Description
Comfort, collected for each eye	Up to Day 6	A visual analogue scale will be used

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026