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Clinical Trials/NCT00673764
NCT00673764
Completed
Not Applicable

The Effect of Systane Ultra Lubricant Eye Drops (FID 112903) on Visual Performance

Alcon Research1 site in 1 country48 target enrollmentMay 2008
ConditionsDry Eye

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Dry Eye
Sponsor
Alcon Research
Enrollment
48
Locations
1
Primary Endpoint
Time at Best Corrected Visual Acuity
Status
Completed
Last Updated
14 years ago

Overview

Brief Summary

To evaluate the effect of 2 different lubricant eye drops on visual function of patients with dry eye

Registry
clinicaltrials.gov
Start Date
May 2008
End Date
June 2008
Last Updated
14 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Documented diagnosis of dry eye
  • Must not have worn contact lenses for 12 hours prior to Day 1

Exclusion Criteria

  • Age related

Outcomes

Primary Outcomes

Time at Best Corrected Visual Acuity

Time Frame: 15 minutes, 45 minutes, and 90 minutes post-dose

Measuring length of time patient can maintain their best vision while completing a computer task. Performed at 15 minutes, 45 minutes, and 90 minutes post-dose. Corrected visual acuity means the patient can wear glasses or contacts if needed such that the measure is performed with the patient seeing the best that they can.

Secondary Outcomes

  • Functional Blink Rate Time (Time Between Blinks)(15 minutes, 45 minutes, and 90 minutes post-dose)

Study Sites (1)

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