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

This study has been completed.

Sponsored by: Allergan
Information provided by: Allergan
ClinicalTrials.gov Identifier: NCT00243711
  Purpose

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.


Condition Intervention Phase
Dry Eye
Drug: Carboxymethylcellulose sodium and Glycerin
Phase II
Phase III

ChemIDplus related topics:   Tetrahydrozoline    Tetrahydrozoline hydrochloride    Carboxymethylcellulose    Glycerol   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Treatment, Randomized, Double-Blind, Active Control, Parallel Assignment, Safety/Efficacy Study

Further study details as provided by Allergan:

Primary Outcome Measures:
  • Dry Eye Symptoms

Secondary Outcome Measures:
  • Ocular surface damage, tear stability, tear production

Estimated Enrollment:   300

  Eligibility
Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No

Criteria

Inclusion Criteria:

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

Exclusion Criteria:

  • NONE
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00243711

Locations
United States, Missouri
      Warrensburg, Missouri, United States

Sponsors and Collaborators
Allergan

Investigators
Principal Investigator:     Mark Curtis, O.D.     InSight Eyecare    
  More Information


Study ID Numbers:   AG9689-001
First Received:   October 21, 2005
Last Updated:   August 24, 2006
ClinicalTrials.gov Identifier:   NCT00243711
Health Authority:   United States: Food and Drug Administration

Study placed in the following topic categories:
Glycerol
Tetrahydrozoline

ClinicalTrials.gov processed this record on October 09, 2008




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