[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Centre Hospitalier Eure-Seine\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":64},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,41],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":29,"lastUpdatePostDateStruct":30,"startDateStruct":33,"completionDateStruct":35,"leadSponsor":37,"locationsCount":40},"100491871","impact-of-remote-care-in-patients-diagnosed-with-thromboembolic-disease-of-low-risk-100491871",false,"NCT05684770","Impact of Remote Care in Patients Diagnosed With Thromboembolic Disease of Low Risk","Evaluation of Feasibility and Impact of Remote Care in Patients With Thromboembolic Disease of Low Risk","TEVEDOM","Inclusion Criteria:\n\n* patients identified in the emergency department with a thromboembolic disease, with a deep vein thrombosis or pulmonary embolism with a low risk of mortality according to recommendations\n* affiliated or beneficiary of social protection\n\nExclusion Criteria:\n\n* patient having a severe obstruction syndrome, a thromboembolic disease already under treatment or a suspicion of thrombocytopenia induced by heparin\n* patient with an active hemorrhage or a major risk of hemorrhage, a renal severe failure, comorbidities such as cancer, or the impossibility to organise a consultation or a patient in a non favorable medico-social context\n* patient with a caval thrombosis\n* patient suffering of a disease at hemorrhagic risk or neurosurgery intervention done in the last month or other surgery in the last 15 days prior to inclusion\n* patient with contraindication of direct oral anticoagulants, such as bitherapy with antiplatelet agent, imidazoles, macrolides, antiretroviral treatments or an anti-phospholipid syndrome\n* patient that lives in an area not covered by internet\n* patient that has no primary care physician\n* patient not able to understand the study (language, psychological problem) or not able to read or write\n* patient under legal protection","ALL","18 Years",{"count":20,"type":21},50,"ESTIMATED","INTERVENTIONAL",[24],"NA","The goal of this clinical trial is to learn about the feasibility and impact of remote care in patients diagnosed with thromboembolic disease of low risk. The main questions it aims to answer are:\n\n* the evaluation of feasibility of organisation between different healthcare professionals (hospital physicians, primary care physician) at 6 months and 1 year\n* the evaluation of complication rate, hospitalisation related to thromboembolic disease rate, compliance to treatment rate at 6 months and 1 year Participants will receive indication of treatment according to national recommendations. Additionnally, they will receive for the length of study a 4G tablet in order to fill questionnaires, learn information about their drugs (patient education), have a remote consultation and evaluate treatment compliance.",[27],"Thromboembolic Disease","RECRUITING","2025-09-09",{"date":31,"type":32},"2025-09-15","ACTUAL",{"date":34,"type":21},"2025-09",{"date":36,"type":21},"2028-03",{"name":38,"class":39},"Centre Hospitalier Eure-Seine","OTHER",1,{"id":42,"slug":43,"hasResults":11,"nctId":44,"briefTitle":45,"officialTitle":45,"acronym":46,"eligibilityCriteria":47,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":48,"targetDuration":4,"studyType":22,"phases":50,"briefSummary":51,"conditions":52,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":56,"lastUpdatePostDateStruct":57,"startDateStruct":59,"completionDateStruct":61,"leadSponsor":63,"locationsCount":40},"100593996","evaluation-of-the-impact-of-virtual-reality-on-sedation-use-in-patients-undergoing-regional-anesthesia-for-scheduled-orthopedic-surgery-100593996","NCT07013695","Evaluation of the Impact of Virtual Reality on Sedation Use in Patients Undergoing Regional Anesthesia for Scheduled Orthopedic Surgery","VIRTUALR","Inclusion Criteria:\n\n* Signed informed consent\n* Patient affiliated with or benefiting from a social security system\n* Patient aged 18 years or older\n* Patient requiring regional anesthesia for scheduled orthopedic surgery of the upper or lower limb\n\nExclusion Criteria:\n\n* Patient refusal to participate in the study\n* Device interfering with the surgical or anesthetic procedure\n* Premedication before arrival in the operating room\n* Psychiatric or cognitive disorders, communication disorders\n* Patient unable to understand the study (language barrier, psychological issues)\n* Emergency surgery",{"count":49,"type":21},164,[24],"The VIRTUALR study evaluates the effect of virtual reality combined with hypnosis on anxiety in patients undergoing orthopedic surgery under regional anesthesia. Patients are randomly assigned to two groups: one group receiving virtual reality and a control group without the device. Anxiety and satisfaction questionnaires are used to compare the two groups.",[53,54,55],"Orthopedic Procedure","Anesthesia","Sedation","2025-06-02",{"date":58,"type":32},"2025-06-10",{"date":60,"type":32},"2024-07-18",{"date":62,"type":21},"2025-07-19",{"name":38,"class":39},""]