An Evaluation of the Daytime Use of an Investigational Lubricant Eye Drop

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT01139372

Enrollment

Registered

2010-06-08

Start date

2010-05-31

Completion date

2010-06-30

Last updated

2012-02-02

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, artificial tears

Brief summary

The purpose of this study is to describe the subjective assessments of an investigational lubricant eye drop.

Interventions

OTHERFID 115958D (Lubricant Eye Drop)

1 drop in each eye at least twice daily

Study design

Allocation

NON_RANDOMIZED

Intervention model

SINGLE_GROUP

Primary purpose

TREATMENT

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* Documented diagnosis of dry eye * Current use of Refresh Liquigel, GenTeal Gel Drops or Refresh Celluvisc at least twice daily

Exclusion criteria

* Must not have worn contact lenses within 7 days preceding enrollment * Must not have had punctal plugs inserted within 30 days preceding enrollment

Design outcomes

Primary

Measure	Time frame
Daytime Use Assessment: I would use this product at bedtime for my dry eye symptoms Likert scale (i.e. strongly disagree, disagree, neither disagree nor agree, agree, strongly agree)	Day 7

Outcome results

None listed

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