Vernal Keratoconjunctivitis Clinical Trial
Official title:
Multicenter, Randomised, Double Masked, Controlled Studies on the Efficacy of Cyclosporine Eye Drop Treatment in Preventing Vernal Keratoconjunctivitis (VKC) Relapses and in Treating the Acute Phase.
This interventional study aims to evaluate the efficacy of Cyclosporine eye drop treatment in preventing relapses of Vernal Keratoconjunctivitis (VKC) and in treating the acute phases of the disease.
Vernal keratoconjunctivitis (VKC) is a severe allergic disease, characterised by chronic
ocular surface inflammation with seasonal relapses. Active phases of VKC require treatment
with topical steroids to control inflammation and corneal damage that may lead to impairment
of visual function and severe ocular discomfort. To date, safe and effective therapies in
preventing relapses and controlling active phases of VKC are not available. Few controlled
trials have used topical Cyclosporine A (CsA) for the treatment of VKC. The present
multicenter, double-masked, randomised, controlled clinical trial will allow to obtain
further data on the safety and efficacy of topical treatment with Cyclosporine in patients
affected by VKC. Moreover, this study will evaluate the efficacy of topical CsA in both
preventing the relapses of VKC and controlling the active phases of the disease. It is
important to highlight that Cyclosporine eye drops are not currently commercially available
in Italy and must be custom-made by specialized pharmacies. As VKC mostly affects young
patients, it influences their daily life and their social interactions. Moreover, the severe
signs and symptoms of the disease result in frequent ophthalmologic controls, influencing
school activities of children and working days for their parents with a relevant economic
cost for the National Health System.
Comparisons: Efficacy of Cyclosporine A 0.05% eye-drops in preventing VKC relapses compared
to standard antiallergic (Ketotifen fumarate 0.025% eye-drops) treatment, and efficacy of
Cyclosporine A 0.1% eye-drops in controlling acute phases compared to antiinflammatory
(Desametasone 0.15% eye drops) treatments.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
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