A Multi-Center Randomized Study to Evaluate the Efficacy and Safety of an Investigational Lubricant Eye Drop

Status

Completed

Phases

Phase 2Phase 3

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT00243711

Enrollment

286

Registered

2005-10-25

Start date

2005-09-30

Completion date

2006-04-30

Last updated

2011-05-30

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 efficacy, safety and acceptability of an investigational lubricant eye drop in subjects with dry eye will be evaluated in comparison with currently-available lubricant eye drops.

Interventions

DRUGCarboxymethylcellulose sodium and Glycerin

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

TREATMENT

Masking

DOUBLE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* Mild, Moderate, or Severe Dry Eye Symptoms and current eye drop use; * Reduced tear stability or tear production

Exclusion criteria

* NONE

Design outcomes

Primary

Measure	Time frame
Dry Eye Symptoms	—

Secondary

Measure	Time frame
Ocular surface damage, tear stability, tear production	—

Countries

United States

Outcome results

None listed

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