Acute Comfort of Lubricant Eye Drops FID 112903
1 other identifier
interventional
20
1 country
1
Brief Summary
To evaluate the acute comfort and blurring profile between two artificial tears in dry eye patients.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started May 2008
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 1, 2008
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2008
CompletedStudy Completion
Last participant's last visit for all outcomes
May 1, 2008
CompletedFirst Submitted
Initial submission to the registry
May 2, 2008
CompletedFirst Posted
Study publicly available on registry
May 7, 2008
CompletedResults Posted
Study results publicly available
March 10, 2010
CompletedFebruary 2, 2012
January 1, 2012
Same day
May 2, 2008
September 10, 2009
January 31, 2012
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Drop Comfort Upon Instillation
Drop comfort grading scale is a scale from 0 to 9, with 0 meaning most comfortable and 9 meaning most uncomfortable.
Three minutes
Study Arms (2)
Lubricant Eye Drops FID 112903
EXPERIMENTALLubricant Eye Drops FID 112903 1 drop each eye one time
Optive Lubricant Eye Drops
ACTIVE COMPARATOROptive Lubricant Eye Drops 1 drop each eye 1 time
Interventions
Lubricant Eye Drops FID 112903 1 drop each eye 1 time
Eligibility Criteria
You may qualify if:
- Documented diagnosis of dry eye
- Must not have worn contact lenses for 1 week preceding enrollment
You may not qualify if:
- Age related
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Alcon Researchlead
Study Sites (1)
Mansfield
Mansfield, Texas, 76134, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Results Point of Contact
- Title
- Alcon Clinical
- Organization
- Alcon Research, Ltd.
Publication Agreements
- PI is Sponsor Employee
- No
- Restriction Type
- OTHER
- Restrictive Agreement
- Yes
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- QUADRUPLE
- Who Masked
- PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- CROSSOVER
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
May 2, 2008
First Posted
May 7, 2008
Study Start
May 1, 2008
Primary Completion
May 1, 2008
Study Completion
May 1, 2008
Last Updated
February 2, 2012
Results First Posted
March 10, 2010
Record last verified: 2012-01