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A Human Factors Study to Evaluate a Novel Intracanalicular Insertion Device in Healthy Subjects

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DataMed2026-07-12 收录
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This is an open-label, multi-center, bilateral, human factors study designed to evaluate the utilization and safety of a novel intracanalicular insertion device in healthy subjects and to evaluate the concentration of DEXTENZA in tears. Each subject's participation is expected to last for approximately 1 month from the DEXTENZA insertion.

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ClinicalTrials.gov
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