Dry Eye Syndromes Clinical Trial
Official title:
Post-approval Study to Assess the Effectiveness of LAMELLEYE vs Comparator for the Treatment of Dry Eye Symptoms in Patients With Primary Sjögren's Syndrome
Single-blind, randomised, single centre, 2-way crossover pilot study to investigate the effectiveness of LAMELLEYE for the treatment of dry eye symptoms in patients with primary Sjögren's Syndrome.
The study is a 2-way crossover design comprising 2 treatments: the CE-marked LAMELLEYE dry
eye drops, and a CE-marked comparator product. All Participants will be allocated to a
treatment group in a random order.
The study design allows observations to be made between the treatments at both an intra- and
inter-patient level regarding relationships between the patient's disease specific quality of
life, symptoms and adverse events, and satisfaction with treatments.
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