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									<identifier>oai:www.peertechzpublications.org:10.17352/2455-1414.000096</identifier>
									<datestamp>2022-05-17</datestamp>
									<setSpec>PTZ.JCRO:VOL9</setSpec>
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									<oai_dc:dc xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:mml="http://www.w3.org/1998/Math/MathML" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
										<dc:title>
										Evaluation of clinical efficacy and safety of Bibrocathol 2% eye ointment in the treatment of Chronic Blepharoconjunctivitis
										</dc:title><dc:creator>Elena Yani</dc:creator><dc:creator> Sergey Astakhov</dc:creator><dc:creator> Vladimir Brzheskiy</dc:creator><dc:creator> Evgeniy Egorov</dc:creator><dc:creator> Alexey Seleznev</dc:creator><dc:creator> Dorothea Groß</dc:creator><dc:creator>Heidi Opitz</dc:creator><dc:description>&lt;p&gt;Purpose: To assess the efficacy and safety of bibrocathol 2% eye ointment in patients with chronic blepharoconjunctivitis.&amp;nbsp;&lt;/p&gt;&lt;p&gt;Materials and methods: This was a multi-center, randomized, double-masked, placebo-controlled, parallel-group, phase III study. Patients with chronic blepharoconjunctivitis were randomized to apply either bibrocathol 2% (n = 100) or placebo (n = 100) three times a day for 14 days. The primary efficacy endpoint was the change from baseline to Day 15(+1 day) in the total score of signs summarizing the investigators’ assessment of the severity of lid oedema, lid erythema, debris, hyperemia, and pouting of Meibomian glands based on slit-lamp examination (modified Intention-to-treat (mITT) set). Safety endpoints included visual acuity, intraocular pressure, and adverse events. Investigators and patients performed an overall assessment of treatment tolerability.&lt;/p&gt;&lt;p&gt;Results: On Day 15(+1 day) the least square (LS) mean change from baseline in the total sum score of signs was -8.62 (95% CI: -9.16; -8.08) in the bibrocathol group and -6.00 (95%CI: -6.54; -5.45) in the placebo group. The LS means the difference between treatment groups was statistically significant in favor of bibrocathol (-2.63 [95% CI: -3.36, -1.89], p &amp;lt; 0.001). Bibrocathol was statistically significantly superior to placebo in reduction of the individual ocular signs scores and the patient’s-assessed ocular discomfort severity (p &amp;lt; 0.001). No safety issues were observed concerning visual acuity, intraocular pressure, and the occurrence of adverse events.&lt;/p&gt;&lt;p&gt;Conclusions: The study showed superior efficacy of two weeks of treatment with bibrocathol versus placebo in reducing signs and symptoms of chronic blepharoconjunctivitis. Treatment with bibrocathol 2% eye ointment was safe and well-tolerated.&lt;/p&gt;</dc:description>
										<dc:publisher>Journal of Clinical Research and Ophthalmology - Peertechz Publications</dc:publisher>
										<dc:date>2022-05-17</dc:date>
										<dc:type>Research Article</dc:type>
										<dc:identifier>https://doi.org/10.17352/2455-1414.000096</dc:identifier>
										<dc:language>en</dc:language>
										<dc:rights>Copyright © Elena Yani et al.</dc:rights>
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