Dry Eye Disease Clinical Trial
Verified date | August 2020 |
Source | Bausch & Lomb Incorporated |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Efficacy study of ecabet ophthalmic solution in dry eye disease
Status | Completed |
Enrollment | 183 |
Est. completion date | September 12, 2008 |
Est. primary completion date | September 12, 2008 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Diagnosed with dry eye disease Exclusion Criteria: - Dry eye disease secondary to surgery |
Country | Name | City | State |
---|---|---|---|
United States | ISTA Pharmaceuticals, Inc. | Irvine | California |
Lead Sponsor | Collaborator |
---|---|
Bausch & Lomb Incorporated |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Mean Change From Baseline in Lacrimation Assessed by Schirmer's Test | The Schirmer's test is used determine if tear glands produce enough tears to keep eyes adequately moist. Calibrated strips of a non-toxic filter paper are used. One free end is placed within the lower eyelid. At the conclusion of the test, the paper strip is removed from the lower eyelid and the amount of wetting of the paper strip is measured. | 43 days |
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