[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"sonography\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:sonography":25},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,44,79],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":23,"conditions":24,"keywords":27,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":4},"100615170","sonographic-evaluation-of-ovarian-masses-by-orads-system-100615170",false,"NCT07289126","Sonographic Evaluation of Ovarian Masses by ORADS System","Sonographic Evaluation of Ovarian Masses by ORADS System in Woman's Health Hospital","Inclusion Criteria:\n\n* Any female patient with ovarian cyst or mass during routine trans-abdominal or pelvic US\n* Age between 18 and 70 years.\n\nExclusion Criteria:\n\n* Refusal of patients to filling consent.\n* Patient with a previous history of the operated ovarian lesion\n* Patient missed during follow-up or not provided pathology report.\n* Pregnancy.\n* Patients with functional ovarian masses ( e.g functional cysts )","FEMALE","18 Years","70 Years",{"count":20,"type":21},80,"ESTIMATED","OBSERVATIONAL","This observational study will evaluate how well an ultrasound scoring system called O-RADS can distinguish between benign (non-cancerous) and malignant (cancerous) ovarian masses in women aged 18 to 70 years. Women who are found to have an ovarian cyst or mass during routine pelvic or transabdominal ultrasound at Women's Health Hospital will be invited to participate and will receive standard care, including detailed transvaginal ultrasound, MRI when indicated, surgery if needed, and histopathology (tissue examination). The main question is how accurately O-RADS ultrasound categories predict the final tissue diagnosis; the study will also look at how ultrasound findings relate to MRI results in characterizing ovarian masses.",[25,26],"Sonography","Ovarian Mass",[28,29,30,31],"ovarian masses","ORADS system","Ovarian-Adnexal Reporting and Data System Ultrasound","sonography","NOT_YET_RECRUITING","2025-12-04",{"date":35,"type":36},"2025-12-17","ACTUAL",{"date":38,"type":21},"2026-01",{"date":40,"type":21},"2027-02",{"name":42,"class":43},"Assiut University","OTHER",{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":49,"acronym":4,"eligibilityCriteria":50,"healthyVolunteers":11,"sex":51,"minAge":17,"maxAge":4,"enrollmentInfo":52,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":54,"conditions":55,"keywords":62,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":69,"lastUpdatePostDateStruct":70,"startDateStruct":72,"completionDateStruct":74,"leadSponsor":76,"locationsCount":78},"100565526","gastric-emptying-time-in-traumatic-injuries-100565526","NCT06643325","Gastric Emptying Time in Traumatic Injuries","Gastric Point-of-care Sonography with Focus on Gastric Emptying Time in Patients with Traumatic Injuries. a Prospective Observational Study","Inclusion Criteria:\n\n* relevant traumatic injury\n\nExclusion Criteria:\n\n* life-threatening traumatic injury (immediate treatment is necessary)\n* Underage\n* Known pregnancy","ALL",{"count":53,"type":21},200,"The investigators plan to do serial sonographic examinations of the gastric antrum (quantity, quality) to estimate the gastric emptying time and dependant factors after traumatic injurys.",[56,57,25,58,59,60,61],"Anesthesia","Gastric Ultrasound","Point of Care Ultrasound (POCUS)","Regurgitation","Pulmonary Aspiration During Anesthetic Induction","Trauma Patients",[63,64,65,66,67],"point of care ultrasound","gastric ultrasound","trauma patients","aspiration","anesthesia","RECRUITING","2024-10-14",{"date":71,"type":36},"2024-10-16",{"date":73,"type":36},"2023-02-01",{"date":75,"type":21},"2025-09-30",{"name":77,"class":43},"Kantonsspital Winterthur KSW",1,{"id":80,"slug":81,"hasResults":11,"nctId":82,"briefTitle":83,"officialTitle":84,"acronym":85,"eligibilityCriteria":86,"healthyVolunteers":11,"sex":87,"minAge":17,"maxAge":4,"enrollmentInfo":88,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":90,"conditions":91,"keywords":95,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":97,"lastUpdatePostDateStruct":98,"startDateStruct":100,"completionDateStruct":101,"leadSponsor":103,"locationsCount":78},"100543157","prevalence-of-synovitis-in-patients-with-haemophilia-a-100543157","NCT06352216","Prevalence of Synovitis in Patients With Haemophilia A","Prevalence of Synovitis in Adult Patients With Haemophilia A in Germany and Austria","SynoPrev","Inclusion Criteria:\n\n* Participants (≥ 18 years old) suffering from moderate or severe haemophilia A, also with inhibitor or joint replacement\n* Complete documentation of hemophilia severity, treatment history (past 12 months), and bleeding events (past 12 months), inhibitor status (at time of enrollment and in past medical history)\n* Submitted written consent to participate in the study\n\nExclusion Criteria:\n\n* Patients suffering from other bleeding disorders conflicting with the research question\n* Patients in clinical studies with investigational drugs","MALE",{"count":89,"type":21},300,"The aim of this study is to evaluate the prevalence of synovitis in adult patients with haemophilia A.",[92,93,94,25],"Haemophilia A","Synovitis","Hemophilia Arthropathy",[93,92,96],"Prevalence","2024-04-15",{"date":99,"type":36},"2024-04-16",{"date":97,"type":36},{"date":102,"type":21},"2027-03",{"name":104,"class":43},"University Hospital, Bonn"]