[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"cardiac\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:cardiac":25},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,5,0,[8,39,75,96,125],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":23,"conditions":24,"keywords":4,"overallStatus":26,"whyStopped":4,"lastUpdateSubmitDate":27,"lastUpdatePostDateStruct":28,"startDateStruct":31,"completionDateStruct":33,"leadSponsor":35,"locationsCount":38},"100639321","spectral-precise-image-study-for-coronary-artery-100639321",false,"NCT07620457","Spectral Precise Image Study for Coronary Artery","Image Quality Evaluation of Coronary CT Angiography Using Deep Learning-Based Spectral Precise Image Reconstruction","Inclusion Criteria:\n\n1. Datasets from Patients who underwent spectral coronary CT angiography (CCTA).\n2. Datasets from study participants with age ≥ 18 years old.\n3. Scan parameters that meet the criteria defined in the 5.4.3.\n\nExclusion Criteria:\n\n1. The clinical data information is considered incomplete after evaluation by the investigator.\n2. The investigator determined that poor image quality (e.g. obvious artifacts, missing critical scan layers) would not satisfy post-processing analysis.\n3. Data of patients deemed inappropriate for inclusion after evaluation by the investigator.",true,"ALL","18 Years",{"count":20,"type":21},200,"ESTIMATED","OBSERVATIONAL","This is a single-center, comparative, observational, retrospective data study. Datasets from patients who underwent spectral coronary CT angiography (CCTA) for suspected coronary artery disease (CAD) or other diagnosis needs as part of their routine clinical evaluation will be included.",[25],"Cardiac","NOT_YET_RECRUITING","2026-05-27",{"date":29,"type":30},"2026-06-02","ACTUAL",{"date":32,"type":21},"2026-06-01",{"date":34,"type":21},"2026-12-31",{"name":36,"class":37},"Philips Clinical & Medical Affairs Global","INDUSTRY",1,{"id":40,"slug":41,"hasResults":11,"nctId":42,"briefTitle":43,"officialTitle":44,"acronym":4,"eligibilityCriteria":45,"healthyVolunteers":11,"sex":17,"minAge":46,"maxAge":47,"enrollmentInfo":48,"targetDuration":4,"studyType":50,"phases":51,"briefSummary":53,"conditions":54,"keywords":59,"overallStatus":64,"whyStopped":4,"lastUpdateSubmitDate":65,"lastUpdatePostDateStruct":66,"startDateStruct":68,"completionDateStruct":70,"leadSponsor":72,"locationsCount":38},"100582981","erector-spinae-block-versus-combined-pecto-intercostal-and-recto-intercostal-fascial-plane-block-in-cardiac-surgery-100582981","NCT06870383","Erector Spinae Block Versus Combined Pecto-intercostal and Recto-intercostal Fascial Plane Block in Cardiac Surgery","Analgesic Efficacy of Erector Spinae Plane Block Versus Combined Pecto-intercostal and Recto-intercostal Fascial Plane Block in Patients Undergoing Cardiac Surgery: A Randomized Comparative Trial","Inclusion Criteria:\n\n* Age from 21 to 65 years.\n* Both sexes.\n* Scheduled for open heart surgery with cardiopulmonary bypass and midline sternotomy.\n\nExclusion Criteria:\n\n* History of chronic pain or Long-term or recent use of opioids.\n* History of allergy to local anesthetic drugs.\n* Ejection fraction of left ventricle less than 30%.\n* History of psychiatric diseases or any neurological disorders.\n* Pre-existing major organ dysfunction as hepatic or renal failure.","21 Years","65 Years",{"count":49,"type":21},66,"INTERVENTIONAL",[52],"NA","The aim of this study is to compare the analgesic effects of ultrasound-guided bilateral erector spinae plane block versus ultrasound-guided bilateral combined Pecto-intercostal fascial plane block and recto-intercostal fascial plane block in patients undergoing cardiac surgery.",[55,56,57,25,58],"Erector Spinae Plane Block","Pecto-intercostal Fascial Plane Block","Recto-intercostal Fascial Plane Block","Surgery",[60,61,62,63,25],"Analgesic","Erector","Pectointercostal","Rectointercostal","RECRUITING","2026-03-14",{"date":67,"type":30},"2026-03-17",{"date":69,"type":30},"2025-03-20",{"date":71,"type":21},"2026-12-20",{"name":73,"class":74},"Tanta University","OTHER",{"id":76,"slug":77,"hasResults":11,"nctId":78,"briefTitle":79,"officialTitle":79,"acronym":4,"eligibilityCriteria":80,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":81,"enrollmentInfo":82,"targetDuration":4,"studyType":50,"phases":84,"briefSummary":85,"conditions":86,"keywords":4,"overallStatus":26,"whyStopped":4,"lastUpdateSubmitDate":87,"lastUpdatePostDateStruct":88,"startDateStruct":90,"completionDateStruct":92,"leadSponsor":94,"locationsCount":38},"100619447","blood-flow-restriction-resistance-exercise-and-cardiac-cycle-dynamics-100619447","NCT07344740","Blood Flow Restriction Resistance Exercise and Cardiac Cycle Dynamics","Inclusion Criteria:\n\n* Generally healthy\n\nExclusion Criteria:\n\n* Uncontrolled hypertension\n* Peripheral vascular disease\n* Lymphedema\n* Sickle cell anemia\n* Heart failure\n* Stroke history\n* Heart attack history\n* Rheumatoid arthritis\n* Chronic kidney disease\n* Diabetes\n* Severe neuropathy\n* Any condition that may make blood flow restriction resistance exercise riskier like history of blood clots\n* Use of coagulant therapy\n* Susceptible to blood clots\n* Obesity","50 Years",{"count":83,"type":21},40,[52],"Blood flow restriction resistance exercise uses partial vascular occlusion of a limb during low weight resistance exercises to stimulate muscle strengthening and growth. This is commonly used during rehabilitation from an injury. Because blood flow in and out of the limbs is decreased, this may have consequences for blood flow through the heart. The purpose of this study will be to test cardiac dynamics during blood flow restriction resistance exercise to determine if cardiac blood flow is impacted. It is hypothesized that both non-BFR exercise and BFR exercise will increase heart rate shortening various cardiac cycle parameters, but BFR exercise will increase the isovolumetric contraction time vs non-BFR exercise due to an increase in total peripheral resistance. It is also hypothesized that BFR exercise will lower early ventricular filling parameters due to lower venous return.",[25],"2026-02-11",{"date":89,"type":30},"2026-02-13",{"date":91,"type":21},"2026-02-01",{"date":93,"type":21},"2028-01-01",{"name":95,"class":74},"Montclair State University",{"id":97,"slug":98,"hasResults":11,"nctId":99,"briefTitle":100,"officialTitle":100,"acronym":4,"eligibilityCriteria":101,"healthyVolunteers":16,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":102,"targetDuration":4,"studyType":50,"phases":104,"briefSummary":105,"conditions":106,"keywords":110,"overallStatus":26,"whyStopped":4,"lastUpdateSubmitDate":115,"lastUpdatePostDateStruct":116,"startDateStruct":118,"completionDateStruct":120,"leadSponsor":122,"locationsCount":38},"100623710","ai-generated-video-feedback-to-improve-technical-skills-in-coronary-artery-bypass-grafting-100623710","NCT07400172","AI-Generated Video Feedback to Improve Technical Skills in Coronary Artery Bypass Grafting","Inclusion Criteria:\n\n* Baseline AI-assessed technical performance ranked in the lower 50% within the scoring system in CAMERA study (NCT06739005)\n\nExclusion Criteria:\n\n* Unwilling to attend",{"count":103,"type":21},100,[52],"This study aims to evaluate whether targeted video feedback generated by an artificial intelligence (AI)-based surgical performance assessment model can support improvement in technical skills among cardiac surgeons performing coronary artery bypass grafting (CABG). This is a single-group, self-controlled, pre-post interventional study. Participating surgeons will submit a baseline CABG surgical video, which will be assessed by both an AI model and blinded human expert raters using standardized scoring criteria. Based on the AI assessment, surgeons will receive personalized video feedback highlighting operative steps associated with lower technical performance. After a one-month self-directed review period, a follow-up CABG surgical video will be submitted and evaluated using the same process. Changes in human-rated technical skill scores between baseline and follow-up will be used to assess the potential educational impact of AI-generated video feedback.",[25,107,108,109],"Surgery (Cardiac)","Education","Artificial Intelligence (AI)",[111,112,113,114],"Coronary Artery Bypass Grafting","Surgical Education","Video-Based Feedback","Artificial Intelligence","2026-02-03",{"date":117,"type":30},"2026-02-10",{"date":119,"type":21},"2026-01-31",{"date":121,"type":21},"2026-04-30",{"name":123,"class":124},"China National Center for Cardiovascular Diseases","OTHER_GOV",{"id":126,"slug":127,"hasResults":11,"nctId":128,"briefTitle":129,"officialTitle":130,"acronym":4,"eligibilityCriteria":131,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":132,"targetDuration":4,"studyType":50,"phases":134,"briefSummary":135,"conditions":136,"keywords":140,"overallStatus":26,"whyStopped":4,"lastUpdateSubmitDate":145,"lastUpdatePostDateStruct":146,"startDateStruct":148,"completionDateStruct":150,"leadSponsor":152,"locationsCount":38},"100622802","a-usability-study-of-a-multi-channel-ecg-monitoring-device-100622802","NCT07388355","A Usability Study of a Multi-channel ECG Monitoring Device","WearLinq eWave Patch Study","Inclusion Criteria:\n\n* Adult \\>18 years old and able to consent\n* Capable of using a smartphone app\n* Willing to shave patch area if needed\n\nExclusion Criteria:\n\n* Planning to undergo an MRI during the study period\n* Known allergic reaction to adhesives or hydrogels or with family history of adhesive skin allergies, or any other dermatological conditional that could confound placement or results\n* Presence of pacemaker, ICD or other implanted electronic devices\n* Open wounds, lesions or infected or inflamed areas of skin at the placement site (left-center of chest\u002Fsternum)\n* Pregnant or intending to become pregnant during the course of the study",{"count":133,"type":21},500,[52],"This study it to evaluate the usability of the WearLinq eWave patch in a general adult population.",[137,138,139,25],"Healthy Adult Participants","Heart Disease","Arrythmia",[141,142,143,144],"Electrocardiogram","ECG","EKG","Cardiac diagnostic","2026-01-29",{"date":147,"type":30},"2026-02-05",{"date":149,"type":21},"2026-02",{"date":151,"type":21},"2027-12",{"name":153,"class":37},"Wearlinq"]