The clinical investigation #1122 is a Post Market Clinical Follow Up Study on the EC marked medical device Reinnerva/Lubristil +G, sterile eye drops, compared to Vismed medical device, sterile eye drops, to demonstrate the clinical performance and tolerability of Reinnerva/Lubristil +G to stabilize the lacrimal film and improve the ocular surface condition in the cases of quali-quantitative alterations of the tear film .
Age range
18 Years – 80 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Clinical Performance and Benefit
Timeframe: From enrollment to the end of treatment at 30 and 60 days.
Clinical Performance and Benefit
Timeframe: From enrollment to the end of treatment at 30 and 60 days.
Clinical Performance and Benefit
Timeframe: From enrollment to the end of treatment at 30 and 60 days.
Clinical Performance and Benefit
Timeframe: From enrollment to the end of treatment at 30 and 60 days.
Clinical Performance and Benefit
Timeframe: From enrollment to the end of treatment at 30 and 60 days.
Safety/Tolerability
Timeframe: From enrollment to the end of treatment at 30 and 60 days.