: Post Marketing, Single Arm, Observational Clinical Registry to Evaluate Safety and Efficacy of 0.9% Sodium Chloride Eye Wash in all comers real-world population - Not applicable

Amanta Healthcare Limited0 个研究点目标入组 188 人开始时间: 待定最近更新: 2021年11月24日

试验速览

暂无简介。

•Inclusion Criteria:
•1. Patients above >=18 years of age.
•2. Patients who are able to give voluntary, written informed consent to participate in this clinical investigation and from whom consent has been obtained.
•3. Patients having moderate to severe symptoms suggestive of conditions such as irritation, discomfort, burning, stinging and itching due to loose foreign material in the eyes wherein the study product would be prescribed by Investigator as part of standard of care.
•4. Patients who have been prescribed study product by Investigator as part of standard of care (SOC) practice and consent has been provided by patient post prescription of study product on the same day.

•Exclusion Criteria:
•1. Patients having any ocular diseases (corneal abrasion, ocular infection, foreign body trapping or ocular trauma), present or past, other than dry eye
•2. History of ocular surgery
•3. Patients using contact lens or topic treatments other than tear substitutes
•4. History of intolerance or hypersensitivity to any component of the study medications
•5. Patients participating in any other clinical trial during study
•6. Pregnant/lactating women during study period.

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