Dry Eye Disease Clinical Trial
Official title:
A Multi-Center, Double-Masked, Randomized, Placebo-Controlled, Dose-Ranging Study of Multiple Ocular Instillations of INS365 Ophthalmic Solution vs. Placebo in Subjects With Dry Eye Disease
Verified date | November 2016 |
Source | Merck Sharp & Dohme Corp. |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Food and Drug Administration |
Study type | Interventional |
The purpose of this trial is to compare the effectiveness and safety of INS365 Ophthalmic Solution with Placebo when applied topically in subjects with dry eye disease.
Status | Completed |
Enrollment | 500 |
Est. completion date | September 2002 |
Est. primary completion date | September 2002 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - best corrected visual acuity in both eyes of at least +0.7 - six-month documented history of dry eye disease - at least mild severity in 2 of the 4 dry eye symptoms - unanesthetized Schirmer score of less than or equal to 7mm - corneal fluorescein staining of greater than or equal to 4 (out of 15) Exclusion Criteria: - nasally stimulated Schirmer score of less than 3mm in subjects with an initial Schirmer score of 0mm - ongoing contact lens wear - current topical ophthalmic medication use |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Merck Sharp & Dohme Corp. |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | change in dry eye testing measures and symptoms | |||
Secondary | change in dry eye testing measures and symptoms |
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