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Clinical Trials/ISRCTN44290046
ISRCTN44290046
Completed
Not Applicable

Additive effect of preservative-free sodium hyaluronate 0.1% in treatment of dry eye syndrome with diquafosol 3% eyedrops

Bucheon St Mary's Hospital (South Korea)0 sites150 target enrollmentMay 27, 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Dry eye syndrome
Sponsor
Bucheon St Mary's Hospital (South Korea)
Enrollment
150
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
May 27, 2014
End Date
TBD
Last Updated
11 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Bucheon St Mary's Hospital (South Korea)

Eligibility Criteria

Inclusion Criteria

  • 1\. Low tear film break\-up time (tBUT) (\<5 seconds)
  • 2\. Low Schirmer I score (10 mm/5 minutes without anesthesia)
  • 3\. Mild corneal punctate fluorescein staining (staining score of \=1\) in either eye (scale 0 \~ 3\)
  • 4\. At least 21 years old

Exclusion Criteria

  • 1\. History of ocular injury, infection, non\-dry eye ocular inflammation, trauma, or surgery within the prior 6 months
  • 2\. Presence of uncontrolled systemic disease

Outcomes

Primary Outcomes

Not specified

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