[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100589993":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":30,"centralContacts":34,"locations":40,"responsibleParty":53,"collaborators":55,"id":59,"slug":60,"hasResults":61,"nctId":62,"briefTitle":63,"officialTitle":64,"acronym":19,"eligibilityCriteria":65,"healthyVolunteers":61,"sex":66,"minAge":67,"maxAge":19,"enrollmentInfo":68,"targetDuration":19,"studyType":71,"phases":72,"briefSummary":74,"conditions":75,"keywords":19,"overallStatus":42,"whyStopped":19,"lastUpdateSubmitDate":77,"lastUpdatePostDateStruct":78,"startDateStruct":81,"completionDateStruct":83,"leadSponsor":85,"locationsCount":86},{"fullName":5,"class":6},"NYU Langone Health","OTHER",[8,15],{"label":9,"type":10,"description":11,"interventionNames":12},"Rivaroxaban + Atorvastatin","EXPERIMENTAL","Participants assigned to this arm will receive rivaroxaban 2.5mg twice daily + atorvastatin 80mg daily for 6 months.",[13,14],"Drug: Rivaroxaban","Drug: Atorvastatin",{"label":16,"type":17,"description":18,"interventionNames":19},"Usual Care","NO_INTERVENTION","Participants assigned to usual care will continue all clinically indicated therapies as prescribed by their treating physicians.",null,[21,26],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":19},"DRUG","Rivaroxaban","Rivaroxaban 2.5mg will be orally administered twice daily for 6 months.",[9],{"type":22,"name":27,"description":28,"armGroupLabels":29,"otherNames":19},"Atorvastatin","Atorvastatin 80mg will be orally administered daily for 6 months.",[9],[31],{"name":32,"affiliation":5,"role":33},"Nathaniel R. Smilowitz, MD, MS","PRINCIPAL_INVESTIGATOR",[35],{"name":36,"role":37,"phone":38,"phoneExt":19,"email":39},"Nathaniel Smilowitz","CONTACT","212-263-5656","Nathaniel.Smilowitz@nyulangone.org",[41],{"facility":5,"status":42,"city":43,"state":43,"zip":44,"country":45,"countryCode":46,"cosmosGeoPoint":47,"geoPoint":52,"contacts":19},"RECRUITING","New York","10016","United States","US",{"type":48,"coordinates":49},"Point",[50,51],-74.00597,40.71427,{"lat":51,"lon":50},{"type":54,"investigatorFullName":19,"investigatorTitle":19,"investigatorAffiliation":19,"oldNameTitle":19,"oldOrganization":19},"SPONSOR",[56],{"name":57,"class":58},"National Heart, Lung, and Blood Institute (NHLBI)","NIH","100589993","early-phase-1-post-operative-biomarker-guided-precision-medicine-for-cardiovascular-risk-reduction-100589993",false,"NCT06961630","Post-Operative Biomarker-Guided Precision Medicine For Cardiovascular Risk Reduction","A Pilot Randomized Trial of Post-Operative Biomarker-Guided Precision Medicine With Rivaroxaban and Atorvastatin for Cardiovascular Risk-Reduction","Inclusion Criteria:\n\n1. Adults ≥45 years\n2. Underwent major non-cardiac surgery requiring ≥1 overnight inpatient stay in the prior 14 days\n3. Myocardial injury after noncardiac surgery, defined as a post-operative troponin ≥ 99th percentile upper reference limit \\[URL\\], with rise\u002Ffall \\>20% indicative of acute myocardial injury.\n4. Ability to provide informed consent\n\nExclusion Criteria:\n\n1. Expected survival \\\u003C6 months\n2. Hemorrhagic disorder\n3. Surgeon feels it is unsafe to initiate low-dose anticoagulation within 14 days of surgery\n4. Indication for oral anticoagulation at discharge\n5. Indication for dual antiplatelet therapy at discharge\n6. Patient already receiving or planned to receive moderate or high-intensity statin\n7. Contraindication to high-intensity statin\n8. Contraindication to rivaroxaban\n9. End stage kidney disease on hemodialysis\n10. Acute liver failure or decompensated cirrhosis\n11. Pregnancy","ALL","45 Years",{"count":69,"type":70},50,"ESTIMATED","INTERVENTIONAL",[73],"EARLY_PHASE1","The goal of this pilot study is to assess enrollment feasibility of a randomized trial of direct oral anticoagulant and high-intensity statin therapy versus usual care in patients with Myocardial Injury after Noncardiac Surgery (MINS). The primary aims of this study are to assess feasibility, study drug adherence, and optimize study design (entry criteria, study endpoints, sample size calculation, site selection) and recruitment strategies for the future multicenter randomized clinical trial studying biomarker-based care in post-operative patients at elevated cardiovascular (CV) risk.",[76],"Myocardial Injury After Noncardiac Surgery","2026-03-31",{"date":79,"type":80},"2026-04-06","ACTUAL",{"date":82,"type":80},"2025-10-07",{"date":84,"type":70},"2027-03-31",{"name":5,"class":6},1]