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AL-15469A for the Treatment of Bacterial Conjunctivitis
This study is ongoing, but not recruiting participants.
Sponsored by: Alcon Research
Information provided by: Alcon Research
ClinicalTrials.gov Identifier: NCT00331916
  Purpose

The purpose of the study is to determine whether AL-15469A is safe and effective in the treatment of bacterial conjunctivitis.


Condition Intervention Phase
Bacterial Conjunctivitis
Drug: quinolone
Phase III

U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study
Official Title: AL-15469A for the Treatment of Bacterial Conjunctivitis

Further study details as provided by Alcon Research:

Primary Outcome Measures:
  • Clinical cure and microbiological success

Secondary Outcome Measures:
  • Individual signs and symptoms of bacterial conjunctivitis at each visit

Estimated Enrollment: 600
Study Start Date: November 2005
  Eligibility

Ages Eligible for Study:   1 Month and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Signs & Symptoms of conjunctivitis

Exclusion Criteria:

  • Under 1 mo. age
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00331916

Locations
United States, Texas
US
Fort Worth, Texas, United States, 76134
Sponsors and Collaborators
Alcon Research
Investigators
Study Director: Stella Robertson, Ph.D. Study Director
  More Information

Study ID Numbers: C-04-38
Study First Received: May 30, 2006
Last Updated: September 10, 2007
ClinicalTrials.gov Identifier: NCT00331916  
Health Authority: United States: Food and Drug Administration

Study placed in the following topic categories:
Bacterial Infections
Eye Infections, Bacterial
Conjunctivitis, Bacterial
Eye Diseases
Eye Infections
Conjunctivitis
Conjunctival Diseases

Additional relevant MeSH terms:
Infection

ClinicalTrials.gov processed this record on January 15, 2009