A post market clinical follows up prospective study to evaluate safety and performance of Preservative Free Eye Preparations (Preservative Free Eye Drops with Calendula Extract plus Hamamelis Extract

Stericon Pharma Private Limited0 个研究点目标入组 144 人开始时间: 待定最近更新: 2024年8月19日

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•At the time of screening and usage of the product all subjects must meet the following criteria for inclusion into the study and the subjects will receive the prescribed eye drops from the PI/CO-PI by a medical practitioner. The inclusion criteria for the subjects for this study are as follows:
•-Subjects who experience Irritation, Itchiness, discomfort of eyes due to the continuous use of computer/TV/exposed pollution/dry environment
•-Subjects wearing contact lenses who experience dryness, Itchiness, discomfort of eyes due to the continuous use of computer/TV/exposed pollution/dry environment

•The below Subjects are excluded from the study:
•-Subjects who are not willing to participate in the study
•-Anyone with known allergic reaction to Sodium chloride eye drops
•-Subjects with existing eye infection
•-Subjects undergone recent (6 weeks) cataract surgery who are on other eye medication

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