A Patient Reported Ocular Comfort Assessment Comparing Bepreve to Lastacaft

NCT01339507 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 25

Last updated 2016-01-27

No results posted yet for this study

Summary

The purpose of this study is to evaluate the comfort of BEPREVE compared to LASTACAFT after instillation.

Conditions

  • Allergic Conjunctivitis

Sponsors & Collaborators

  • Bausch & Lomb Incorporated

    collaborator INDUSTRY
  • Cunningham, Derek N., O.D., P.A.

    lead INDIV

Principal Investigators

  • Derek Cunningham, OD · Dell Laser Consultants

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2011-04-30
Primary Completion
2011-05-31
Completion
2011-06-30

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 NCT01339507 on ClinicalTrials.gov