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Study of BUT measurement method

Phase 1
Conditions
Dry eye disease
Registration Number
JPRN-jRCTs062220022
Lead Sponsor
Sakane Yuri
Brief Summary

We examined the effectiveness of the MR6000 for dry eye screening. One hundred healthy volunteers were interviewed for dry eye symptoms (DEQS), measured for Ring BUT (RBUT; seconds) which is the MR6000 non-invasive BUT, and measured fluorescein BUT (FBUT; seconds). The results of 45 people were analyzed, and the RBUT demonstrated a good correlation with the FBUT. Tthe noninvasive assessment of tear film stability using the MR6000 was found to be a useful tool for dry eye screening in clinical practice.

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
100
Inclusion Criteria

The eligible subjects are >=20 years and written informed consent.

Exclusion Criteria

1.Active ocular infection
2.Corneal ulcer

Study & Design

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