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Study of Diquafosol Tetrasodium Ophthalmic Solution in Subjects With Dry Eye Disease
This study has been completed.
First Received: November 22, 2006   Last Updated: November 24, 2006   History of Changes
Sponsored by: Inspire Pharmaceuticals
Information provided by: Inspire Pharmaceuticals
ClinicalTrials.gov Identifier: NCT00403975
  Purpose

The purpose of this trial is to assess the effectiveness and safety of 2% diquafosol tetrasodium ophthalmic solution versus placebo following 6 weeks of treatment in subjects with mild to moderate dry eye disease.


Condition Intervention Phase
Dry Eye Disease
Drug: diquafosol tetrasodium ophthalmic solution, 2%
Phase III

MedlinePlus related topics: Eye Diseases
Drug Information available for: Diquafosol
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study
Official Title: A Multi-Center, Parallel Group, Double-Masked, Randomized, Placebo-Controlled Study of Multiple Ocular Instillations of Diquafosol Tetrasodium Ophthalmic Solution, 2% in Subjects With Dry Eye Disease

Further study details as provided by Inspire Pharmaceuticals:

Primary Outcome Measures:
  • Change in dry eye testing measures

Secondary Outcome Measures:
  • Change in dry eye testing measures and symptoms

Estimated Enrollment: 520
Study Start Date: June 2004
  Eligibility

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

Inclusion Criteria:

  • best corrected visual acuity in both eyes of at least +0.7
  • six-month documented history of dry eye disease
  • as least mild severity in 1 of the 5 dry eye symptoms
  • corneal fluorescein staining of greater than or equal to 3 and less than or equal to 6 (out of 15)

Exclusion Criteria:

  • permanent conjunctival goblet cell loss or scarring conditions
  • ongoing contact lens wear
  • current topical ophthalmic medication use
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00403975

Locations
United States, Florida
Center for Excellence in Eye Care
Miami, Florida, United States, 33176
Sponsors and Collaborators
Inspire Pharmaceuticals
  More Information

No publications provided

Study ID Numbers: 03-109
Study First Received: November 22, 2006
Last Updated: November 24, 2006
ClinicalTrials.gov Identifier: NCT00403975     History of Changes
Health Authority: United States: Food and Drug Administration

Study placed in the following topic categories:
Eye Diseases

Additional relevant MeSH terms:
Eye Diseases

ClinicalTrials.gov processed this record on May 07, 2009