{"id":4684,"date":"2023-07-04T07:46:06","date_gmt":"2023-07-04T06:46:06","guid":{"rendered":"https:\/\/dart.datariverweb.com\/iEnter?glossary=protokoll"},"modified":"2023-07-26T15:55:00","modified_gmt":"2023-07-26T14:55:00","slug":"protokoll","status":"publish","type":"glossary","link":"https:\/\/dart.datariverweb.com\/iEnter?glossary=protokoll&lang=sv","title":{"rendered":"Protokoll"},"content":{"rendered":"\n<p>Ett dokument som beskriver forskningsplanen innan studien genomf\u00f6rs. Protokollet \u00e4r utformat f\u00f6r att beskriva studiens metoder och f\u00f6rfaranden, s\u00e5 att den kan replikeras. I protokollet ska f\u00f6ljande information tydligt anges: anledningen till att studien genomf\u00f6rs, definitionen av m\u00e5lgruppen (urvalskriterierna), antalet deltagare som ska ing\u00e5, beskrivningen av de behandlingar som studeras, planerade tester och diagnostiska f\u00f6rfaranden, l\u00e4kemedel och deras doser, studiens l\u00e4ngd och deltagarnas uppgifter. Ibland utarbetar forskarna protokollet i samarbete med patienterna eller deras f\u00f6retr\u00e4dare. Varje kliniskt studieprotokoll m\u00e5ste registreras i s\u00e4rskilda institutionella databaser (USA <a rel=\"noreferrer noopener\" href=\"http:\/\/www.clinicaltrials.gov\" data-type=\"URL\" data-id=\"www.clinicaltrials.gov\" target=\"_blank\">www.clinicaltrials.gov<\/a> , EU <a rel=\"noreferrer noopener\" href=\"http:\/\/www.clinicaltrialsregister.eu\/\" data-type=\"URL\" data-id=\"www.clinicaltrialsregister.eu\/\" target=\"_blank\">www.clinicaltrialsregister.eu\/<\/a> ).<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Ett dokument som beskriver forskningsplanen innan studien genomf\u00f6rs. Protokollet \u00e4r utformat f\u00f6r att beskriva studiens metoder och f\u00f6rfaranden, s\u00e5 att den kan replikeras. I protokollet ska f\u00f6ljande information tydligt anges: anledningen till att studien genomf\u00f6rs, definitionen av m\u00e5lgruppen (urvalskriterierna), antalet deltagare som ska ing\u00e5, beskrivningen av de behandlingar som studeras, planerade tester och diagnostiska f\u00f6rfaranden, l\u00e4kemedel och deras doser, studiens l\u00e4ngd och deltagarnas uppgifter. Ibland utarbetar forskarna protokollet i samarbete med patienterna eller deras f\u00f6retr\u00e4dare. Varje kliniskt studieprotokoll m\u00e5ste registreras i s\u00e4rskilda institutionella databaser (USA www.clinicaltrials.gov , EU www.clinicaltrialsregister.eu\/ ).<\/p>\n","protected":false},"author":5,"featured_media":0,"parent":0,"template":"","glossary-cat":[],"class_list":["post-4684","glossary","type-glossary","status-publish","hentry"],"blocksy_meta":{"styles_descriptor":{"styles":{"desktop":"","tablet":"","mobile":""},"google_fonts":[],"version":5}},"aioseo_notices":[],"related_terms":"Protokollet","external_url":"","internal_reference_id":"","_links":{"self":[{"href":"https:\/\/dart.datariverweb.com\/iEnter\/index.php?rest_route=\/wp\/v2\/glossary\/4684","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/dart.datariverweb.com\/iEnter\/index.php?rest_route=\/wp\/v2\/glossary"}],"about":[{"href":"https:\/\/dart.datariverweb.com\/iEnter\/index.php?rest_route=\/wp\/v2\/types\/glossary"}],"author":[{"embeddable":true,"href":"https:\/\/dart.datariverweb.com\/iEnter\/index.php?rest_route=\/wp\/v2\/users\/5"}],"version-history":[{"count":1,"href":"https:\/\/dart.datariverweb.com\/iEnter\/index.php?rest_route=\/wp\/v2\/glossary\/4684\/revisions"}],"predecessor-version":[{"id":4685,"href":"https:\/\/dart.datariverweb.com\/iEnter\/index.php?rest_route=\/wp\/v2\/glossary\/4684\/revisions\/4685"}],"wp:attachment":[{"href":"https:\/\/dart.datariverweb.com\/iEnter\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=4684"}],"wp:term":[{"taxonomy":"glossary-cat","embeddable":true,"href":"https:\/\/dart.datariverweb.com\/iEnter\/index.php?rest_route=%2Fwp%2Fv2%2Fglossary-cat&post=4684"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}