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Evaluation of the changes of quantity and quality of tears by diquafosol sodium instillatio

Phase 4
Conditions
Dry eye
Registration Number
JPRN-UMIN000005233
Lead Sponsor
Department of Ophthalmology, Kyoto Prefectural University of Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
60
Inclusion Criteria

Not provided

Exclusion Criteria

Anyone who is considered to be inappropriate for this study (ex. Any allergic history to diquafosol sodium and artificial tear, women who are under pregnant or lactation period)

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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