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Main
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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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17 October 2012 |
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Main ID: |
NCT01417013 |
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Date of registration:
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12/08/2011 |
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Primary sponsor: |
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Public title:
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Comparative Efficacy of SYSTANE® ULTRA vs Optive™ in Improving Tear Film Break-up Time
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Scientific title:
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A Comparative Efficacy of SYSTANE® ULTRA vs Optive™ in Improving Tear Film Break-up Time |
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Date of first enrolment:
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July 2011 |
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Target sample size:
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0 |
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Recruitment status: |
Withdrawn |
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URL:
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http://clinicaltrials.gov/show/NCT01417013 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Single Blind (Investigator), Primary Purpose: Treatment
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Countries of recruitment
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United States
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Corrected VA of 0.6 LogMar or better OU
Exclusion:
- Topical ocular medication use
- Presence of Ocular conditions (blepharitis, conjunctival infections, etc)
Age minimum:
18 Years
Age maximum:
N/A
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Dry Eye
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Intervention(s)
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Other: Optive
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Other: Systane Ultra
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Primary Outcome(s)
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TBUT
[Time Frame: 14 Days]
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Secondary ID(s)
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SMA-10-07
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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