[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100570888":3},{"organization":4,"armGroups":7,"interventions":17,"overallOfficials":23,"centralContacts":28,"locations":34,"responsibleParty":53,"collaborators":11,"id":55,"slug":56,"hasResults":57,"nctId":58,"briefTitle":59,"officialTitle":60,"acronym":61,"eligibilityCriteria":62,"healthyVolunteers":57,"sex":63,"minAge":11,"maxAge":11,"enrollmentInfo":64,"targetDuration":11,"studyType":67,"phases":68,"briefSummary":70,"conditions":71,"keywords":11,"overallStatus":37,"whyStopped":11,"lastUpdateSubmitDate":74,"lastUpdatePostDateStruct":75,"startDateStruct":78,"completionDateStruct":80,"leadSponsor":82,"locationsCount":83},{"fullName":5,"class":6},"University of Sao Paulo General Hospital","OTHER",[8,12],{"label":9,"type":10,"description":11,"interventionNames":11},"Usual care","NO_INTERVENTION",null,{"label":13,"type":14,"description":11,"interventionNames":15},"Interventional care","ACTIVE_COMPARATOR",[16],"Behavioral: Tempos Certos protocol",[18],{"type":19,"name":20,"description":21,"armGroupLabels":22,"otherNames":11},"BEHAVIORAL","Tempos Certos protocol","Improve the enhanced recovery by using the Tempos Certos Protocol by the multiprofissional team , using interventions known by science and recommended by scientists.",[13],[24],{"name":25,"affiliation":26,"role":27},"Gabrielle B Borgomoni, bsc, PhD student","Instituto do coração","PRINCIPAL_INVESTIGATOR",[29],{"name":30,"role":31,"phone":32,"phoneExt":11,"email":33},"Omar A V Mejia, md, PhD","CONTACT","555+(11) 2661-5014","omarvmejia@gmail.com",[35],{"facility":36,"status":37,"city":38,"state":38,"zip":39,"country":40,"countryCode":41,"cosmosGeoPoint":42,"geoPoint":47,"contacts":48},"Hc Da Fmusp Instituto Do Coracao Incor Sao Paulo","RECRUITING","São Paulo","5403000","Brazil","BR",{"type":43,"coordinates":44},"Point",[45,46],-46.63611,-23.5475,{"lat":46,"lon":45},[49],{"name":50,"role":31,"phone":51,"phoneExt":11,"email":52},"Elaine Lagonegro, BSC","(11) 2661-5000","gestaodeprojetos@incor.usp.br",{"type":54,"investigatorFullName":11,"investigatorTitle":11,"investigatorAffiliation":11,"oldNameTitle":11,"oldOrganization":11},"SPONSOR","100570888","study-to-evaluate-the-impact-of-the-recovery-pathway-on-postoperative-leght-of-stay-in-coronary-artery-bypass-surgery-100570888",false,"NCT06713096","Study to Evaluate the Impact of the Recovery Pathway on Postoperative Leght of Stay in Coronary Artery Bypass Surgery","Prospective and Randomized Study to Evaluate the Impact of the Recovery Pathway on Postoperative Leght of Stay in Coronary Artery Bypass Surgery","KAMAY","Inclusion Criteria:\n\n* Adult patients (\\>18 years old)\n* Undergoing isolated coronary artery bypass grafting (CABG) with elective or urgent status\n* Signed informed consent form (ICF)\n\nExclusion Criteria:\n\n* Emergency patients\n* Severe ventricular dysfunction (ejection fraction \\\u003C30%)\n* Renal impairment (creatinine clearance \\\u003C30 mL\u002Fmin)\n* Atrial fibrillation or need for oral anticoagulation\n* Moderate-to-severe anemia (hematocrit \\\u003C32%)\n* STS risk score \\>4%\n* Patient and\u002For family disagreement with the protocol\n* Failure to sign the informed consent form","ALL",{"count":65,"type":66},128,"ESTIMATED","INTERVENTIONAL",[69],"NA","This randomized and prospective trial aims to evaluate the implementation of a rapid recovery protocol for coronary artery bypass grafting (CABG) in a hospital serving patients from the Brazilian Unified Health System (Sistema Único de Saúde - SUS). The study will compare outcomes between two groups: patients receiving care under the rapid recovery protocol and those following the standard institutional care.\n\nPrimary Objective:\n\nCompare postoperative hospital stay between the rapid recovery group and the usual care group.\n\nSecondary Objectives:\n\nAssess morbidity and mortality between both groups.\n\nEvaluate patient satisfaction using validated tools.\n\nAnalyze incremental costs associated with both approaches.\n\nAssess healthcare teams' learning progression regarding the protocol (Kirkpatrick method).\n\nEvaluate adherence to rapid recovery protocol metrics by healthcare teams.\n\nMeasure changes in patient safety culture among healthcare professionals.\n\nHypothesis:\n\nThe null hypothesis assumes no difference in hospital stay between the two groups. The alternative hypothesis suggests that the rapid recovery protocol will reduce hospital stay compared to the standard care. Previous findings from Mejia et al. (2022) indicated a 40% reduction in postoperative hospital stay (from 13 to 7.8 days) for cardiac surgery patients under a rapid recovery protocol at the Heart Institute (InCor HCFMUSP).\n\nThis trial will provide critical insights into the applicability of enhanced recovery after surgery (ERAS) principles in cardiac surgery within the context of public healthcare, aiming to improve outcomes and optimize resource use.",[72,73],"Enhanced Recovery After Surgery","Quality Improvement","2024-11-26",{"date":76,"type":77},"2024-12-03","ACTUAL",{"date":79,"type":77},"2021-11-25",{"date":81,"type":66},"2025-12",{"name":5,"class":6},1]