[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"ct-scan\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:ct-scan":65},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,40],{"id":9,"slug":4,"hasResults":10,"nctId":11,"briefTitle":12,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":10,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":17,"targetDuration":4,"studyType":20,"phases":21,"briefSummary":23,"conditions":24,"keywords":4,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":28,"lastUpdatePostDateStruct":29,"startDateStruct":32,"completionDateStruct":34,"leadSponsor":36,"locationsCount":39},"100607713",false,"NCT07192133","Evaluation of CT-XPI","Evaluation of Computed Tomography X-ray-Pulsatility Index (CT-XPI)","Inclusion Criteria:\n\n* Age 18 years or older\n* Able to sign and date the informed consent form\n* Will undergo a clinically-indicated CT exam of the head, neck, chest, abdomen, pelvis, or extremities\n\nExclusion Criteria:\n\n* Pregnant or lactating\n* In need of urgent or emergent care\n* Have any conditions that, in the opinion of the PI or designee, would interfere with the evaluation of the results or constitute a health hazard for the participant","ALL","18 Years",{"count":18,"type":19},30,"ESTIMATED","INTERVENTIONAL",[22],"PHASE2","The goal of this clinical trial is to learn if a new computed tomography (CT) lung perfusion imaging method is as effective as standard of care (SOC) CT imaging. The main question it aims to answer is:\n\n* Does the new contrast-free method provide more information about lung perfusion than SOC?\n\nParticipants will undergo a 30 minute chest CT.",[25,26],"CT Scan","Computed Tomography","RECRUITING","2026-06-09",{"date":30,"type":31},"2026-06-10","ACTUAL",{"date":33,"type":31},"2026-01-26",{"date":35,"type":19},"2026-12",{"name":37,"class":38},"University of Wisconsin, Madison","OTHER",1,{"id":41,"slug":4,"hasResults":10,"nctId":42,"briefTitle":43,"officialTitle":43,"acronym":4,"eligibilityCriteria":44,"healthyVolunteers":10,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":45,"targetDuration":4,"studyType":47,"phases":4,"briefSummary":48,"conditions":49,"keywords":52,"overallStatus":55,"whyStopped":4,"lastUpdateSubmitDate":56,"lastUpdatePostDateStruct":57,"startDateStruct":59,"completionDateStruct":61,"leadSponsor":63,"locationsCount":4},"100625578","NCT07424456","Comparison Between Triphasic CT Abdomen and EUS-FNB in Characterization of Pancreatic Lesion","Inclusion Criteria:\n\n* \\*Adult patients (age\\>18 years) presenting with focal pancreatic lesions detected on initial imaging.\n\n  * Patients referred for further evaluation by triphasic CT and\u002For EUS-guided biopsy.\n  * Patients able to provide informed consent\n\nExclusion Criteria:\n\n* Previous pancreatic surgery.\n\n  * Known metastatic disease at presentation.\n  * Contraindications to contrast-enhanced CT (e.g. severe renal impairment, contrast allergy)\n  * Contraindications to EUS or biopsy (e.g., coagulopathy uncorrected, severe cardiopulmonary instability).\n  * Pregnancy.",{"count":46,"type":19},50,"OBSERVATIONAL","evaluate the relationship between triphasic CT and EUS findings and the characterization of pancreatic lesions.",[50,25,51],"EUS Guided Biopsy","Pancreatic Lesions Located at the Body or the Tail",[53,54],"Triphasic Ct abdomen vs EUS-FNB","EUS-FNB","NOT_YET_RECRUITING","2026-02-13",{"date":58,"type":31},"2026-02-20",{"date":60,"type":19},"2026-02-01",{"date":62,"type":19},"2027-04-01",{"name":64,"class":38},"Assiut University",""]