[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"dvt---deep-vein-thrombosis\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:dvt---deep-vein-thrombosis":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,41,66],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":24,"conditions":25,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":29,"lastUpdatePostDateStruct":30,"startDateStruct":33,"completionDateStruct":35,"leadSponsor":37,"locationsCount":40},"100593702","clinical-application-of-wearable-ultrasound-sensors-100593702",false,"NCT07009873","Clinical Application of Wearable Ultrasound Sensors","Clinical Application on the R&D Purpose of Wearable Ultrasound Sensors:A Single-Center Prospective Study","Inclusion Criteria:\n\n* Age ≥ 18 yrs and able to consent\n* Relevant diagnosis for study arm (heart failure, lower-limb DVT, or ICU monitoring)\n* Adequate acoustic window and intact skin at sensor site\n\nArm-specific:\n\n* Heart-failure arm: Clinically stable HFrEF or HFpEF on standard therapy\n* DVT arm: Imaging-confirmed lower-limb DVT, anticoagulated or scheduled for intervention\n* ICU arm: ICU\u002Fpost-op patient requiring continuous bedside ultrasound\n\nExclusion Criteria:\n\n* Poor acoustic window preventing interpretable images\n* Local skin infection, open wound, or implant\u002Fhardware blocking sensor\n* Inability to cooperate with monitoring\n\nArm-specific:\n\n* Heart-failure arm: Acute MI or uncontrolled arrhythmia in past 3 months\n* DVT arm: Active bleeding or severe coagulopathy\n* ICU arm: Unstable multi-organ failure precluding safe monitoring",true,"ALL","18 Years","70 Years",{"count":21,"type":22},300,"ESTIMATED","OBSERVATIONAL","This study aims to develop and evaluate a wearable ultrasound imaging sensor for the early diagnosis and real-time monitoring of various diseases, such as cardiovascular conditions and structural abnormalities of superficial organs. With advancements in medical technology, wearable devices have attracted increasing attention for their portability and real-time capabilities.",[26,27],"DVT - Deep Vein Thrombosis","POCUS","RECRUITING","2026-03-18",{"date":31,"type":32},"2026-03-20","ACTUAL",{"date":34,"type":32},"2025-08-15",{"date":36,"type":22},"2026-09-30",{"name":38,"class":39},"Chinese PLA General Hospital","OTHER",1,{"id":42,"slug":43,"hasResults":11,"nctId":44,"briefTitle":45,"officialTitle":46,"acronym":47,"eligibilityCriteria":48,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":49,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":51,"conditions":52,"keywords":54,"overallStatus":56,"whyStopped":4,"lastUpdateSubmitDate":57,"lastUpdatePostDateStruct":58,"startDateStruct":60,"completionDateStruct":62,"leadSponsor":64,"locationsCount":40},"100572396","padua-prediction-score-for-vte-risk-in-thoracic-surgery-patients-100572396","NCT06732726","Padua Prediction Score for VTE Risk in Thoracic Surgery Patients","Assessment of the Padua Prediction Score for Venous Thromboembolism Risk Stratification in Thoracic Surgery Patients: Insights From a Single-Center Cohort Study in Iraq","DVT","Inclusion Criteria:\n\n* Patients who have undergone preoperative Padua Prediction Score assessment.\n* Inpatients with a hospital stay over 3 days\n* Written informed consent obtained from patients or their legal guardians.\n* Availability for postoperative follow-up to assess outcomes like LEVT development or related complications.\n\nExclusion Criteria:\n\n* Preexisting LEVT or pulmonary embolism.\n* Severe Coagulopathy: Patients with inherited or acquired bleeding disorders (e.g., hemophilia, advanced liver disease).\n* receiving any anticoagulation therapy for any reason.\n* patients who did not undergo a postoperative D-dimer test.\n* Incomplete Data: missing essential clinical or laboratory data.\n* Pregnancy: pregnant women or those within six weeks postpartum.\n* Noncompliance: Patients unwilling or unable to adhere to study follow-up protocols.",{"count":50,"type":22},150,"The goal of this observational study is to assess the predictive accuracy of the Padua Prediction Score (PPS) for venous thromboembolism (VTE) risk in thoracic surgery patients.\n\nThe study aims to answer the following question:\n\nDoes the PPS provide a more accurate prediction of VTE risk?\n\nParticipants will:\n\nHave their VTE risk assessed using the PPS during their hospital admission.",[26,53],"VTE (Venous Thromboembolism)",[55],"Padua Prediction Score (PPS)","NOT_YET_RECRUITING","2025-03-16",{"date":59,"type":32},"2025-03-18",{"date":61,"type":22},"2025-04-20",{"date":63,"type":22},"2025-07-15",{"name":65,"class":39},"Al-Nahrain University",{"id":67,"slug":68,"hasResults":11,"nctId":69,"briefTitle":70,"officialTitle":71,"acronym":47,"eligibilityCriteria":72,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":73,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":75,"conditions":76,"keywords":77,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":57,"lastUpdatePostDateStruct":80,"startDateStruct":81,"completionDateStruct":83,"leadSponsor":85,"locationsCount":40},"100572111","predictive-value-of-modified-caprini-score-and-d-dimer-in-managing-lower-limb-venous-thrombosis-in-cardiothoracic-patients-100572111","NCT06729021","Predictive Value of Modified Caprini Score and D-Dimer in Managing Lower Limb Venous Thrombosis in Cardiothoracic Patients","Predictive Efficacy of Modified Caprini Score and D-Dimer for the Evaluation and Management of Lower Extremity Venous Thrombosis Among Cardiothoracic Surgery Patients in Baghdad","Inclusion Criteria:\n\n* Inpatients with a hospital stay over 3 days\n* Written informed consent obtained from patients or their legal guardians.\n* Availability for postoperative follow-up to assess outcomes like LEVT development or related complications.\n\nExclusion Criteria:\n\n* Preexisting LEVT or Pulmonary Embolism: Diagnosed before the index surgery.\n* Severe Coagulopathy: Patients with inherited or acquired bleeding disorders (e.g., hemophilia, advanced liver disease).\n* receiving any anticoagulation therapy for any reason.\n* patients who did not undergo a postoperative D-dimer test.\n* Incomplete Data: missing essential clinical or laboratory data for Modified Caprini Score calculation or D-Dimer measurement.\n* Pregnancy: pregnant women or those within six weeks postpartum.\n* Noncompliance: Patients unwilling or unable to adhere to study follow-up protocols.",{"count":74,"type":22},112,"The goal of this observational study is to evaluate the predictive efficacy of the Modified Caprini Risk Assessment Score and D-Dimer in identifying and managing lower extremity venous thrombosis (LEVT) among cardiothoracic surgery patients in Baghdad. The main questions it aims to answer are:\n\nDoes combining the Modified Caprini Score with D-Dimer improve the accuracy of predicting lower extremity venous thrombosis (LEVT) compared to using each tool independently? Can these tools effectively guide clinical decisions for lower extremity venous thrombosis (LEVT) prevention and management in this patient population?\n\nParticipants will:\n\nUndergo risk assessment for lower extremity venous thrombosis (LEVT) using the Modified Caprini Score and have their D-Dimer levels measured during their hospital stay.\n\nBe monitored for clinical outcomes, including confirmed lower extremity venous thrombosis (LEVT) incidence, need for anticoagulation therapy, and complications such as pulmonary embolism or recurrent thrombosis.",[26],[78,79,47],"Caprini Score","D-Dimer",{"date":59,"type":32},{"date":82,"type":32},"2025-01-20",{"date":84,"type":22},"2025-07-30",{"name":65,"class":39}]