Acute Comfort and Blur of Systane and Optive

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Alcon Research
ClinicalTrials.gov Identifier:
NCT00568386
First received: December 5, 2007
Last updated: January 31, 2012
Last verified: January 2012

December 5, 2007
January 31, 2012
November 2007
Not Provided
Visual Blur [ Time Frame: 3 minutes post dose ] [ Designated as safety issue: No ]
Visual blur profile is a visual scale ranging from 0 (no blur) to 50 (most blurry). Patients were asked to rate there vision on a specific focal point (an object in the room) through 3 minutes.
Drop comfort upon instillation, overall acceptability, three-minute visual blur profile [ Time Frame: 3 minutes ] [ Designated as safety issue: No ]
Complete list of historical versions of study NCT00568386 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
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Acute Comfort and Blur of Systane and Optive
Acute Comfort and Blurring Profile Evaluation Comparing Systane Lubricant Eye Drops to Optive Lubricant Eye Drops

To evaluate drop comfort, acceptability, preference and blur profile between two marketed artificial tears in both dry eye and non-dry eye patient population.

Not Provided
Interventional
Not Provided
Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: Double-Blind
Primary Purpose: Treatment
Dry Eye
  • Other: Systane Lubricant Eye Drops
    Systane Lubricant Eye Drops 1 drop each eye once time
  • Other: Optive Lubricant Eye Drops
    Optive Lubricant Eye Drops 1 drop each eye one time
  • Experimental: Systane Lubricant Eye Drops
    Systane Lubricant Eye Drops 1 drop in each eye one time
    Intervention: Other: Systane Lubricant Eye Drops
  • Active Comparator: Optive Lubricant Eye Drops
    Optive Lubricant Eye Drops 1 drop each one time
    Intervention: Other: Optive Lubricant Eye Drops
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
40
December 2007
Not Provided

Inclusion Criteria:

  • Healthy, normal eyes OR documented diagnosis of dry eye

Exclusion Criteria:

  • Must not have worn contact lenses for 7 days preceding enrollment
Both
18 Years and older
Yes
Contact information is only displayed when the study is recruiting subjects
Not Provided
 
NCT00568386
M-07-02
No
Alcon Research
Alcon Research
Not Provided
Principal Investigator: Mike Christensen Alcon Research
Alcon Research
January 2012

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