{"id":5317,"date":"2022-01-24T11:54:13","date_gmt":"2022-01-24T10:54:13","guid":{"rendered":"http:\/\/10.14.1.26\/website\/klinisch-onderzoek\/"},"modified":"2026-01-15T15:58:58","modified_gmt":"2026-01-15T14:58:58","slug":"klinisch-onderzoek","status":"publish","type":"page","link":"https:\/\/www.stpierre-bru.be\/nl\/klinisch-onderzoek\/","title":{"rendered":"Klinisch onderzoek"},"content":{"rendered":"

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Klinisch onderzoek<\/h1>\n

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De <\/span>eenheid voor Klinisch Onderzoek van de Medische Raad <\/span><\/strong> (EKO) bevordert en organiseert klinische studies. Deze studies worden op initiatief van klinische artsen of farmaceutische firma\u2019s verricht.<\/span><\/p>\n

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Klinisch onderzoek past in het streven van het UMC om de behandeling van pati\u00ebnten te verbeteren en laat toe innoverende alternatieve behandelingen en\/of diagnoses aan te bieden.<\/span><\/h3>\n

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Klinisch onderzoek maakt deel uit van medisch onderzoek.<\/strong>. Er wordt een beroep gedaan op mensen die vrijwillig <\/strong>deelnemen aan zorgvuldig geleide studies. Klinisch onderzoek heeft als doel de behandeling, preventie en diagnose te bevorderen en ziektes van het menselijk lichaam beter te begrijpen. Klinisch onderzoek kan bestaan uit het testen van nieuwe behandelingen en therapie\u00ebn of studies op de lange termijn naar het natuurlijke verloop van een ziekte en de gezondheid.<\/span><\/p>\n

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Klinische studies bevatten criteria die bepalen wie mag deelnemen. Deze zogeheten toelatingscriteria staan vermeld in een document: <\/span>een protocol<\/em>.<\/p>\n

De toelatingscriteria<\/em><\/strong><\/span> bestaat uit twee soorten. De factoren die toelaten dat iemand aan een klinische studie deelneemt, heten <\/span>inclusiecriteria<\/em>. De factoren die iemand uitsluiten, zijn de <\/span>exclusiecriteria<\/em>. Deze criteria zijn gebaseerd op leeftijd, geslacht, het type ziekte en het stadium van de ziekte, de behandelingsantecedenten en andere medische voorwaarden.<\/p>\n

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