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Fluorophotometry Evaluation of Lubricant Eye Drops

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Alcon Research
ClinicalTrials.gov Identifier:
NCT00347854
First received: June 30, 2006
Last updated: November 18, 2016
Last verified: February 2012
June 30, 2006
November 18, 2016
April 2006
April 2006   (Final data collection date for primary outcome measure)
Epithelial permeability to fluorescein
Same as current
Complete list of historical versions of study NCT00347854 on ClinicalTrials.gov Archive Site
tear turnover rate
Same as current
Not Provided
Not Provided
 
Fluorophotometry Evaluation of Lubricant Eye Drops
Fluorophotometry Evaluation of Lubricant Eye Drops FID 105783
The objective of this study is to evaluate the safety and efficacy of exaggerated use of Lubricant Eye Drops in a population of normal subjects by measuring corneal epithelial permeability to fluorescein.
Not Provided
Interventional
Not Provided
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double Blind (Participant, Investigator)
Healthy
  • Other: Systane Free lubricant eye drops
  • Other: Visine Tears Lubricant Eye Drops
  • Other: Refresh Liquigel Lubricant Eye Drops
  • Other: Refresh Plus Lubricant Eye Drops
  • Experimental: FID 105783
    Intervention: Other: Systane Free lubricant eye drops
  • Active Comparator: Visine
    Intervention: Other: Visine Tears Lubricant Eye Drops
  • Active Comparator: Refresh Liquigel
    Intervention: Other: Refresh Liquigel Lubricant Eye Drops
  • Active Comparator: Refresh Plus
    Intervention: Other: Refresh Plus Lubricant Eye Drops
http://www.aaopt.org/evaluation-new-preservation-system-corneal-barrier-function

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
40
April 2006
April 2006   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • Ages 18 and over

Exclusion Criteria:

  • No sodium fluorescein corneal staining at Screening Visit
Sexes Eligible for Study: All
18 Years and older   (Adult, Senior)
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
 
NCT00347854
C-05-06
No
Not Provided
Not Provided
Alcon Research
Alcon Research
Not Provided
Study Director: Mike Christensen Alcon Research
Alcon Research
February 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP