2004
DOI: 10.1016/s0149-2918(04)80065-1
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Clinical efficacy of olopatadine hydrochloride ophthalmic solution 0.2% compared with placebo in patients with allergic conjunctivitis or rhinoconjunctivitis: a randomized, double-masked environmental study

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Cited by 39 publications
(22 citation statements)
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“…Simultaneous analysis of pollen level (frequency based) and pollen period (severity based) was performed to account for influence of environmental variables on clinical differences in ocular itching and redness between treatment groups [52]. Results revealed olopatadine 0.2% was associated with significant reductions in calculated mean scores for ocular itching and redness by pollen level and by pollen period [52]. A similar three-armed trial contrasting olopatadine HCl 0.1% versus ketotifen fumarate 0.025% versus artificial tear substitute in patients with seasonal allergic conjunctivitis.…”
Section: Dual Action Agent Versus Placebo or Dual Action Agentmentioning
confidence: 99%
“…Simultaneous analysis of pollen level (frequency based) and pollen period (severity based) was performed to account for influence of environmental variables on clinical differences in ocular itching and redness between treatment groups [52]. Results revealed olopatadine 0.2% was associated with significant reductions in calculated mean scores for ocular itching and redness by pollen level and by pollen period [52]. A similar three-armed trial contrasting olopatadine HCl 0.1% versus ketotifen fumarate 0.025% versus artificial tear substitute in patients with seasonal allergic conjunctivitis.…”
Section: Dual Action Agent Versus Placebo or Dual Action Agentmentioning
confidence: 99%
“…A. с соавт [17,18]. Было продемон-стрировано, что мононуклеары периферической крови плода способны отвечать на контакт со специфическими аллергенами, начиная с 22 недели гестации, и интенсив-ность ответа возрастает с увеличением гестационного возраста.…”
Section: Issn 1816-5095 (Print); Issn 2500-0845 (Online) Doi: 101800unclassified
“…Олопатадин 0,2% имеет концентрацию олопатадина, в два раза превышающую его концентрацию в известном препарате Опатанол® (олопатадин 0,1%). Препарат Визаллергол® применяют один раз в сутки для лечения зуда и покраснения в об-ласти век, связанных с аллергическим конъюнктивитом [18,19]. Препарат характеризуется длительным сроком действия -до 24 часов [20].…”
Section: Issn 1816-5095 (Print); Issn 2500-0845 (Online) Doi: 101800unclassified
“…the safety and efficacy of olopatadine has been shown in active-and placebo-controlled trials. [47][48][49] the efficacy of olopatadine 0.1 % was compared with levocabastine 0.05 % in a cac study. 50 Subjects were bilaterally challenged with an allergen 27 minutes after topical drug administration, and the first postchallenge assessment was carried out 3 minutes later, or 30 minutes after instillation of the drug.…”
Section: Mechanism Of Action Of Dual-acting Agents In Ocular Allergymentioning
confidence: 99%
“…a 10-week, randomized, placebo-controlled trial to determine the efficacy and safety of 0.2 % olopatadine QD in the treatment of ac or rhinoconjunctivitis was conducted in 260 patients. 48 this environmental study assessed ocular signs and symptoms in terms of frequency (whole-unit scale from 0 to 5) and severity (half-unit scale from 0 to 4); grass pollen counts were also assessed daily. analyses of ocular itching and redness showed that when grass pollen counts were high, a respective 21 % and 14 % of patients in the olopatadine 0.2 % group assessed the frequency of ocular itching and redness as >grade 2 compared with 47 % and 31 % of patients in the placebo group (p<0.001 for ocular itching; p<0.003 for redness, respectively).…”
Section: Mechanism Of Action Of Dual-acting Agents In Ocular Allergymentioning
confidence: 99%