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Efficacy and safety of artificial tears containing Artemia salina extract with dinucleotides for dry eye

dc.contributor.authorCarracedo Rodríguez, Juan Gonzalo
dc.contributor.authorGarcía-Gonzalo, Cristina
dc.contributor.authorPerez-Luque, Maria A.
dc.contributor.authorMartínez-Aguila, Alejandro
dc.contributor.authorCarpena-Torres, Carlos
dc.date.accessioned2025-01-21T16:26:05Z
dc.date.available2025-01-21T16:26:05Z
dc.date.issued2024-04
dc.description.abstractClinical relevance: This clinical trial was conducted as part of the marketing procedures for a medical device comprising artificial tears containing Artemia salina extract with dinucleotides. These molecules previously demonstrated secretagogue properties by enhancing the production of aqueous, mucinous, and lipidic components of the tears. Background: After confirming the efficacy of artificial tears containing Artemia salina extract in an animal model, this study proceeded to evaluate their efficacy and safety on dry eye participants. Methods: A randomised controlled clinical trial was performed on 36 dry eye participants (41.6 ± 20.6 years). Half of the participants were treated with saline solution as a placebo for four weeks, while the other half were treated with artificial tears containing Artemia salina, randomly assigned. After a wash-out period of two weeks, the treatments were crossed for another four weeks. Participants were assessed at baseline and after one week, two weeks, and four weeks. Efficacy variables were: eye dryness frequency (primary), eye comfort, visual satisfaction, tear secretion, tear break-up time, corneal staining, conjunctival staining, and conjunctival hyperaemia. Safety variables were: high- and low-contrast visual acuity, intraocular pressure, and eye fundus images analysis. Results: Compared with the baseline, the saline solution showed no significant changes in any of the studied variables after four weeks of treatment (p ≥ 0.05). However, the topical instillation of the artificial tears with Artemia salina for four weeks significantly improved eye dryness frequency (p = 0.014) and corneal staining (p = 0.010). No systemic or ocular adverse events were reported during the clinical trial. Conclusion: The topical instillation of artificial tears containing Artemia salina in mild to moderate dry eye participants for four weeks slightly improved their symptoms related to eye dryness frequency and reduced corneal damage, with no undesirable side effects observed.
dc.description.departmentDepto. de Optometría y Visión
dc.description.facultyFac. de Óptica y Optometría
dc.description.refereedTRUE
dc.description.statussubmitted
dc.identifier.citationCarracedo G, Garcia-Gonzalo C, Perez-Luque MA, Martinez-Aguila A, Carpena-Torres C. Efficacy and safety of artificial tears containing Artemia salina extract with dinucleotides for dry eye. Clin Exp Optom. 2024 Apr 23:1-7. doi: 10.1080/08164622.2024.2341841. Epub ahead of print. PMID: 38653499.
dc.identifier.doi10.1080/08164622.2024.2341841
dc.identifier.officialurlhttps://doi.org/10.1080/08164622.2024.2341841
dc.identifier.urihttps://hdl.handle.net/20.500.14352/115441
dc.journal.titleClinical and Experimental Optometry
dc.language.isoeng
dc.publisherPubMed
dc.rights.accessRightsrestricted access
dc.subject.cdu617.764
dc.subject.keywordArtemia salina
dc.subject.keywordArtificial tears
dc.subject.keywordDinucleotides
dc.subject.keywordDry eye
dc.subject.keywordPurinergic signalling
dc.subject.ucmÓptica y optometría
dc.subject.unesco3201.09 Oftalmología
dc.titleEfficacy and safety of artificial tears containing Artemia salina extract with dinucleotides for dry eye
dc.typejournal article
dc.type.hasVersionVoR
dspace.entity.typePublication
relation.isAuthorOfPublication97433353-d31b-4cf5-b2c0-47d2e6703fe5
relation.isAuthorOfPublication.latestForDiscovery97433353-d31b-4cf5-b2c0-47d2e6703fe5

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