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This combination ophthalmic solution contains glycerin (0.2%), hypromellose (0.2%), and polyethylene glycol (1.0%), which function as lubricants and demulcents to protect and hydrate the ocular surface. In the clinical trial context provided by Wills Eye Hospital (NCT05514301), this formulation is utilized as a pharmacologically inactive placebo control to evaluate the safety and efficacy of netarsudil 0.02% ophthalmic solution in preventing proliferative vitreoretinopathy (PVR) in patients undergoing repair for rhegmatogenous retinal detachment (RRD). The ingredients work by stabilizing the tear film and providing a protective barrier over the corneal epithelium, thereby reducing irritation and dryness without exerting specific anti-fibrotic or rho-kinase inhibitory effects.
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