Evaluation of Comfort in Subjects With Moderate Dry Eye Disease

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT04830956

Enrollment

Registered

2021-04-05

Start date

2021-06-30

Completion date

2021-11-10

Last updated

2021-11-16

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

Conditions

Dry Eye

Keywords

Dry eye

Brief summary

The purpose of this study is to evaluate the comfort of an ocular lubricant in dry eye subjects. This study will be conducted in Canada and Australia.

Interventions

OTHERFID123238

Lubricant applied to the ocular surface

OTHERSystane Hydration

Drops applied to the ocular surface

Study design

Allocation

RANDOMIZED

Intervention model

CROSSOVER

Primary purpose

OTHER

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

Key Inclusion Criteria: * Able to understand and sign an information consent letter * Willing and able to follow instructions and maintain the appointment schedule * Has dry eye symptoms Key

Exclusion criteria

* Has suffered any ocular injury to either eye in the past 12 weeks * Is pregnant or lactating at the time of enrollment Other protocol-specified inclusion/

Design outcomes

Primary

Measure	Time frame	Description
Change from baseline in comfort rating	Baseline, up to 12 Hours (Day 1, each product)	A visual analogue scale will be used

Countries

Australia

Outcome results

None listed

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