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Safety Evaluation of a New Preservative in a Lubricating Eye Drop

NCT01434277 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 44

Last updated 2011-09-14

No results posted yet for this study

Summary

This study is to evaluate the safety of a new preservative in a lubricant eye drop used four times a day in healthy adults and subjects diagnosed with dry eye.

Conditions

  • Dry Eye Syndromes

Interventions

OTHER

Eye Drops with Experimental Preservative

Glycerin, Hypromellose, Polyethylene glycol 400 with experimental preservative PQ-42

Sponsors & Collaborators

  • Johnson & Johnson Consumer and Personal Products Worldwide

    lead INDUSTRY

Principal Investigators

  • Sherryl Frisch · Johnson & Johnson Consumer and Personal Products Worldwide

Study Design

Allocation
NON_RANDOMIZED
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2011-04-30
Primary Completion
2011-04-30
Completion
2011-04-30

Countries

  • United States

Study Locations

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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 NCT01434277 on ClinicalTrials.gov