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The purpose of this study is to demonstrate that Olopatadine 0.2% is superior to vehicle in the treatment of the signs and symptoms associated with allergic conjunctivitis or rhinoconjunctivitis.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Olopatadine Hydrochloride 0.2% | Experimental | Olopatadine hydrochloride ophthalmic solution, 0.2%, 1 drop in each eye, once-daily in the morning for 6 weeks |
|
| Vehicle | Placebo Comparator | Olopatadine hydrochloride ophthalmic solution vehicle, 1 drop in each eye, once-daily in the morning for 6 weeks |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Olopatadine Hydrochloride Ophthalmic Solution, 0.2% | Drug |
| ||
| Olopatadine Hydrochloride Ophthalmic Solution Vehicle |
| Measure | Description | Time Frame |
|---|---|---|
| Daily ocular itching and redness scores | Up to Day 14 |
| Measure | Description | Time Frame |
|---|---|---|
| Percentage of patients with daily ocular itching and redness scores of 0 | Up to Day 14 |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Alcon, A Novartis Company | Alcon, a Novartis Company | Study Director |
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| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| Result | https://www.ncbi.nlm.nih.gov/pubmed/23379201 |
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| ID | Term |
|---|---|
| D003233 | Conjunctivitis, Allergic |
| ID | Term |
|---|---|
| D003231 | Conjunctivitis |
| D003229 | Conjunctival Diseases |
| D005128 | Eye Diseases |
| D006969 | Hypersensitivity, Immediate |
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| Drug |
Inactive ingredients used as a placebo comparator |
|
| D006967 |
| Hypersensitivity |
| D007154 | Immune System Diseases |