Evaluation of Comfort of Ocular Lubricants in Symptomatic Contact Lens Wearers

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT05741216

Enrollment

Registered

2023-02-23

Start date

2023-05-01

Completion date

2023-10-02

Last updated

2023-10-11

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

Conditions

Dry Eye

Brief summary

The purpose of this study is to evaluate the ocular comfort of 3 ocular lubricants and a comparator.

Detailed description

The expected duration of subject participation is at least 7 days. This study will be conducted in Australia and Canada.

Interventions

OTHEROTF Ocular Lubricant

Ocular lubricant in 1 of 3 test formulations

OTHEROcular Lubricant

Commercially available ocular lubricant

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

TREATMENT

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 * Uses rewetting drops on a regular basis; * 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 specified

Design outcomes

Primary

Measure	Time frame	Description
Ocular comfort	Up to Day 5	Comfort will be rated using a visual analog scale (0-100) from 0-100, where 0=poor and 100=excellent.

Countries

Australia, Canada

Outcome results

None listed

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