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 .
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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.