Status:
COMPLETED
Residence Time Evaluation of Systane Ultra Lubricant Eye Drops vs. Hialid and Saline
Lead Sponsor:
Alcon Research
Conditions:
Dry Eye Syndrome
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
The purpose of this study is to evaluate the ocular retention time of Systane Ultra compared to Hialid and saline.
Eligibility Criteria
Inclusion
- Diagnosed with mild to moderate dry eye as defined in the protocol.
- Able and willing to follow instructions.
- Other protocol-defined inclusion criteria may apply.
Exclusion
- Any medical condition that may affect the results of the study.
- History or evidence of ocular or intraocular surgery within the past six months.
- History of intolerance or hypersensitivity to any component of the study medications.
- Use of concomitant topical ocular medications during the study period.
- Ocular conditions that may preclude safe administration of the test article.
- Unwilling to discontinue contact lens wear during the study period.
- Participation in an investigational drug or device study within 30 days of enrollment.
- Other protocol-defined exclusion criteria may apply.
Key Trial Info
Start Date :
October 1 2010
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
June 1 2011
Estimated Enrollment :
27 Patients enrolled
Trial Details
Trial ID
NCT01252121
Start Date
October 1 2010
End Date
June 1 2011
Last Update
October 30 2012
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