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An Evaluation of the Nighttime Retention of Effect of an Investigational Lubricant Eye Drop (FID 115958D)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01165164
Enrollment
89
Registered
2010-07-19
Start date
2010-06-30
Completion date
2010-07-31
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 night-time use of an investigational lubricant eye drop.

Interventions

1 drop in each eye at bedtime

Sponsors

Alcon Research
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Documented diagnosis of dry eye 2. Current use of an eye ointment or tube gel

Exclusion criteria

1. No nighttime contact lenses wear throughout the study period 2. Must not have had punctal plugs inserted within 30 days preceding enrollment

Design outcomes

Primary

MeasureTime frameDescription
Nighttime Use AssessmentDay 7Nighttime 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)

Outcome results

None listed

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