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A Clinical Evaluation of an Investigational Lubricant Eye Gel (FID 115958D)

NCT01294956 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 147

Last updated 2016-11-18

No results posted yet for this study

Summary

The purpose of this study is to estimate the change in sodium fluorescein staining, as a sign of dry eye, during six weeks of treatment with FID 115958D or Refresh Liquigel.

Conditions

  • Dry Eye

Interventions

OTHER

Lubricant Eye Drop

1 drop in each eye, four times a day for 42 days

OTHER

Refresh Liquigel

1 drop in each eye, four times a day for 42 days

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-01-31
Primary Completion
2011-04-30
Completion
2011-04-30

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01294956 on ClinicalTrials.gov