{"id":9049,"date":"2022-09-16T14:49:00","date_gmt":"2022-09-16T12:49:00","guid":{"rendered":"https:\/\/czecrin.cz\/project\/kh-m-a-r-s\/"},"modified":"2026-01-27T13:58:28","modified_gmt":"2026-01-27T12:58:28","slug":"kh-m-a-r-s","status":"publish","type":"project","link":"https:\/\/czecrin.cz\/en\/project\/kh-m-a-r-s\/","title":{"rendered":"CT M.A.R.S."},"content":{"rendered":"\n<h3 class=\"wp-block-heading has-text-align-center\">CLINICAL TRIAL M.A.R.S.<\/h3>\n\n\n\n<hr class=\"wp-block-separator has-text-color has-black-color has-alpha-channel-opacity has-black-background-color has-background\"\/>\n\n\n\n<div style=\"height:30px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<p class=\"has-text-align-center\">M.A.R.S. is a randomised double-blind placebo-controlled multicentre study of the efficacy and safety of highly diluted atropine collyrium in retarding the development of myopia in children, a phase IIIb study with three parallel arms designed to increase clinical knowledge of the effect of topical application of highly diluted atropine on axial length growth in myopic eyes and to add to experimental knowledge of the efficacy and safety of this application.<\/p>\n\n\n\n<p class=\"has-text-align-center\">The study was initiated by the University Hospital Brno in cooperation with Masaryk University. It is a paediatric clinical trial that will enrol a total of 236 patients in 5 centres in the Czech Republic.<\/p>\n\n\n\n<h6 class=\"wp-block-heading has-text-align-center\">OVERVIEW OF RECRUITMENT<\/h6>\n\n\n\n<p class=\"has-text-align-center\"><strong>Patient recruitment<\/strong> started on <strong>29 June 2022<\/strong> and was completed on <strong>29 August 2024<\/strong>. A total of <strong>236 patients<\/strong> were enrolled in the study.<\/p>\n\n\n\n<p class=\"has-text-align-center\"><strong>Total number of enrolled patients:<\/strong> 236\/236<\/p>\n\n\n\n<h2 class=\"wp-block-heading has-text-align-center\">Important links to the project<\/h2>\n\n\n\n<hr class=\"wp-block-separator has-alpha-channel-opacity\"\/>\n\n\n\n<div style=\"height:30px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<figure class=\"wp-block-table\"><table class=\"has-fixed-layout\"><tbody><tr><td class=\"has-text-align-center\" data-align=\"center\"><strong><a href=\"https:\/\/redcap.med.muni.cz\/\" target=\"_blank\" rel=\"noreferrer noopener\">Access to the REDCap database (for examiners)<\/a><\/strong><\/td><td class=\"has-text-align-center\" data-align=\"center\"><strong><a href=\"https:\/\/www.clinicaltrialsregister.eu\/ctr-search\/search?query=2020-002046-16\" target=\"_blank\" rel=\"noreferrer noopener\">Clinical Trials register &#8211; Search for 2020-002046-16<\/a><\/strong><\/td><td class=\"has-text-align-center\" data-align=\"center\"><strong><a href=\"http:\/\/www.m-a-r-s.cz\/\" target=\"_blank\" rel=\"noreferrer noopener\">Official project website<\/a><\/strong><\/td><\/tr><tr><td class=\"has-text-align-center\" data-align=\"center\"><strong><a href=\"https:\/\/www.heraldopenaccess.us\/openaccess\/myopia-control-in-european-children-study-protocol-and-methodology\" target=\"_blank\" rel=\"noreferrer noopener\">Publications<\/a><\/strong><\/td><td class=\"has-text-align-center\" data-align=\"center\"><strong><a href=\"https:\/\/czecrin.cz\/wp-content\/uploads\/2026\/01\/MARS.pdf\">Document: Transfer of the Clinical Trial to the CTIS portal as of 01 November 2024<\/a><\/strong><\/td><td class=\"has-text-align-center\" data-align=\"center\"><\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n<div style=\"height:100px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<h2 class=\"wp-block-heading has-text-align-center\">Trial documents<\/h2>\n\n\n\n<hr class=\"wp-block-separator has-text-color has-black-color has-alpha-channel-opacity has-black-background-color has-background\"\/>\n\n\n\n<div style=\"height:30px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<figure class=\"wp-block-table\"><table class=\"has-fixed-layout\"><tbody><tr><td class=\"has-text-align-center\" data-align=\"center\"><strong><a href=\"https:\/\/czecrin.cz\/wp-content\/uploads\/2025\/04\/2020-06-23_Schvaleni-Atropine-Collyrium-121234-20.pdf\" target=\"_blank\" rel=\"noreferrer noopener\">Approval of S\u00daKL<\/a><\/strong><\/td><td class=\"has-text-align-center\" data-align=\"center\"><strong><a href=\"https:\/\/czecrin.cz\/wp-content\/uploads\/2025\/04\/2020-11-04_MARS_Souhlasne-stanovisko-MEK-FN-Brno.pdf\" target=\"_blank\" rel=\"noreferrer noopener\">Approval of MEK FN Brno<\/a><\/strong><\/td><td class=\"has-text-align-center\" data-align=\"center\"><strong><a href=\"https:\/\/czecrin.cz\/wp-content\/uploads\/2025\/05\/The-Rationale-of-clinical-trial-1.pdf\" target=\"_blank\" rel=\"noreferrer noopener\">The Rationale of clinical trial<\/a><\/strong><\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n<div style=\"height:20px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<div style=\"height:100px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<h5 class=\"wp-block-heading has-text-align-center\">Contact<\/h5>\n\n\n\n<p class=\"has-text-align-center has-medium-font-size\">Study sponsor:<br>FN Brno | prof. MUDr. Rudolf Autrata, CSc., MBA | <a href=\"mailto:autrata.rudolf@fnbrno.cz\">autrata.rudolf@fnbrno.cz<\/a><\/p>\n\n\n\n<div style=\"height:20px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<p class=\"has-text-align-center has-medium-font-size\">Project manager:<br>Mgr. et Bc. \u0160\u00e1rka Maty\u0161kov\u00e1 | <a href=\"mailto:matyskova@med.muni.cz\">matyskova@med.muni.cz<\/a>  <\/p>\n\n\n\n<div style=\"height:30px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<ul class=\"wp-block-social-links aligncenter is-layout-flex wp-block-social-links-is-layout-flex\"><li class=\"wp-social-link wp-social-link-x  wp-block-social-link\"><a href=\"https:\/\/twitter.com\/intent\/tweet?hashtags=remed%2Cczecrin%2Cclinicaltrials&#038;original_referer=https%3A%2F%2Fczecrin.cz%2F&#038;ref_src=twsrc%5Etfw%7Ctwcamp%5Ebuttonembed%7Ctwterm%5Eshare%7Ctwgr%5E&#038;related=%40czecrin&#038;text=KH%20M.A.R.S.%20-%20Czecrin&#038;url=https%3A%2F%2Fczecrin.cz%2Fprojekty%2Fkh-mars%2F\" class=\"wp-block-social-link-anchor\"><svg width=\"24\" height=\"24\" viewBox=\"0 0 24 24\" version=\"1.1\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" aria-hidden=\"true\" focusable=\"false\"><path d=\"M13.982 10.622 20.54 3h-1.554l-5.693 6.618L8.745 3H3.5l6.876 10.007L3.5 21h1.554l6.012-6.989L15.868 21h5.245l-7.131-10.378Zm-2.128 2.474-.697-.997-5.543-7.93H8l4.474 6.4.697.996 5.815 8.318h-2.387l-4.745-6.787Z\" \/><\/svg><span class=\"wp-block-social-link-label screen-reader-text\">X<\/span><\/a><\/li><\/ul>\n","protected":false},"excerpt":{"rendered":"<p>CLINICAL TRIAL M.A.R.S. M.A.R.S. is a randomised double-blind placebo-controlled multicentre study of the efficacy and safety of highly diluted atropine collyrium in retarding the development of myopia in children, a phase IIIb study with three parallel arms designed to increase clinical knowledge of the effect of topical application of highly diluted atropine on axial length [&hellip;]<\/p>\n","protected":false},"author":5,"featured_media":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"_et_pb_use_builder":"","_et_pb_old_content":"","_et_gb_content_width":"","inline_featured_image":false,"footnotes":""},"project_category":[147,146],"project_tag":[153,154],"class_list":["post-9049","project","type-project","status-publish","hentry","project_category-national-research-projects","project_category-ongoing-clinical-trials","project_tag-pediatrics","project_tag-phase-iii"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.2 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>CT M.A.R.S. &#8226; CZECRIN - \u010cesk\u00e1 n\u00e1rodn\u00ed s\u00ed\u0165 pro podporu klinick\u00e9ho v\u00fdzkumu<\/title>\n<meta name=\"description\" content=\"Effect of dexamethasone in patients with ARDS and COVID-19 - a prospective, multicentre, open-label, randomised controlled trial with parallel groups.COVID-19 is still a major challenge for medical research, with new drugs or possible optimisation of existing drugs being investigated. 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