[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"anatomy\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:anatomy":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,5,0,[8,42,71,95,116],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":4},"100646718","application-of-a-responsive-web-based-sinus-ct-scan-interpretation-training-system-in-clinical-education-100646718",false,"NCT07687992","Application of a Responsive Web-Based Sinus CT Scan Interpretation Training System in Clinical Education","Application of a Responsive Web-Based Sinus CT Scan Interpretation Training System in Clinical Education: A Prospective, Randomized Controlled Trial","Inclusion Criteria:\n\n* Medical students currently in their clinical clerkship or internship phase, or junior physicians currently undergoing standardized residency training;\n* No prior systematic training in specialized otolaryngology-head and neck surgery (ORL-HNS) imaging;\n* Voluntary participation in the study with a signed informed consent form.\n\nExclusion Criteria:\n\n* Inability to access a basic smartphone or computer required for the digital training system;\n* Anticipated inability to complete the intervention, and assessment period (e.g., due to planned prolonged leave of absence).",true,"ALL",{"count":19,"type":20},36,"ESTIMATED","INTERVENTIONAL",[23],"NA","The complex anatomy of the paranasal sinuses and skull base presents a steep learning curve for junior clinicians in otolaryngology. This prospective, randomized controlled trial aims to evaluate the effectiveness of a novel, responsive web-based sinus CT scan interpretation training system compared to traditional educational methods. The study will enroll 36 medical trainees and junior resident physicians with no prior specialized training in otolaryngology imaging.\n\nFollowing a standardized baseline video lecture, participants will be randomized (1:1) into two groups for a one-week rotation period. The intervention group will utilize an interactive, cross-platform web system featuring multi-planar correlations, the CLOSE mnemonic guided reading, and case-based self-assessments. The control group will study using standard digitized text-and-image guidelines and clinical consensus documents. The primary outcome is the objective CT interpretation score, which evaluates the accuracy of identifying anatomical variations and pathological grading (e.g., Lund-Mackay score, osteitis grading) across 10 anonymized clinical cases. Secondary outcomes include interpretation time, diagnostic confidence, and system usability. The findings of this study will provide valuable evidence on whether interactive digital tools can effectively accelerate the learning curve and improve diagnostic accuracy in specialized medical imaging education.",[26,27,28,29],"Education","Diagnostic Imaging","Otolaryngology","Anatomy","NOT_YET_RECRUITING","2026-07-02",{"date":33,"type":34},"2026-07-07","ACTUAL",{"date":36,"type":20},"2026-08-01",{"date":38,"type":20},"2026-09-30",{"name":40,"class":41},"First Affiliated Hospital, Sun Yat-Sen University","OTHER",{"id":43,"slug":44,"hasResults":11,"nctId":45,"briefTitle":46,"officialTitle":47,"acronym":4,"eligibilityCriteria":48,"healthyVolunteers":11,"sex":17,"minAge":49,"maxAge":50,"enrollmentInfo":51,"targetDuration":4,"studyType":53,"phases":4,"briefSummary":54,"conditions":55,"keywords":57,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":61,"lastUpdatePostDateStruct":62,"startDateStruct":64,"completionDateStruct":65,"leadSponsor":67,"locationsCount":70},"100611977","adductor-canal-localization-in-living-and-cadaver-100611977","NCT07247591","Adductor Canal Localization in Living and Cadaver","Determination of Adductor Canal Location by USG Measurements and Cadaver Correlation","Inclusion Criteria:\n\nASA 1-2-3 patients\n\nBMI \\\u003C35\n\nAges 18-65\n\nThose willing to participate in the study\n\nExclusion Criteria:\n\nThose unwilling to participate in the study\n\nPregnant women\n\nBMI \\>35\n\nASA 4-5-6 patients","18 Years","65 Years",{"count":52,"type":20},200,"OBSERVATIONAL","The aim of this study is to define the starting and ending points of the adductor canal in adductor canal block (ACB) applications through distance measurements relative to the anterior superior iliac spine (ASIS) and the adductor tubercle. These measurements are performed using ultrasound (USG) and correlated with cadaveric data.\n\nKey research questions addressed include:\n\n* Can the start and end points of the adductor canal be formulated along a line drawn between the ASIS and the adductor tubercle?\n* Is there a definable relationship between the block application site and anatomical landmarks such as the vastoadductor membrane (VAM), the apex of the femoral triangle, and other adjacent structures that facilitates localization?\n\nBy validating ultrasound measurements with cadaveric findings, the study aims to provide researchers with a more predictable and reliable method for determining the optimal site for adductor canal block administration.",[29,56],"Adductor Canal Block",[58,59,60],"ASIS","ADDUCTOR CANAL","BLOCK","2025-11-22",{"date":63,"type":34},"2025-11-25",{"date":63,"type":20},{"date":66,"type":20},"2026-02-01",{"name":68,"class":69},"Ankara Etlik City Hospital","OTHER_GOV",1,{"id":72,"slug":73,"hasResults":11,"nctId":74,"briefTitle":75,"officialTitle":76,"acronym":4,"eligibilityCriteria":77,"healthyVolunteers":16,"sex":78,"minAge":4,"maxAge":4,"enrollmentInfo":79,"targetDuration":4,"studyType":53,"phases":4,"briefSummary":81,"conditions":82,"keywords":4,"overallStatus":85,"whyStopped":4,"lastUpdateSubmitDate":86,"lastUpdatePostDateStruct":87,"startDateStruct":89,"completionDateStruct":91,"leadSponsor":93,"locationsCount":70},"100602500","placental-characteristics-within-monochorionic-twin-pregnancies-100602500","NCT07124312","Placental Characteristics Within Monochorionic Twin Pregnancies","Placental Characteristics Within Monochorionic Twin Pregnancies: a Prospective Cohort Study.","Inclusion Criteria:\n\n• All consecutive placentas of monochorionic twin pregnancies whereby the placenta is transferred to the pathology department for analysis.\n\nExclusion Criteria:\n\n* Singleton, dichorionic and higher order pregnancies (e.g. triplet).\n* Fetus with known major congenital anomalies or aneuploidy","FEMALE",{"count":80,"type":20},65,"This prospective study aims to collate a comprehensive database of all main monochorionic twin groups to enable comparisons to be made within each twin group and additionally between each group with regards to several placental characteristics, whilst understanding their impact on several fetal outcomes. This study aims to provide new insights in to how the placental architecture influences pregnancy care within the UK pregnancy cohort. Results of this study may impact how clinicians conduct antenatal surveillance for these anatomical placental factors.\n\nPatients of both uncomplicated and complication monochorionic twin groups will be consented at a single site and recruited during the antenatal period. Following delivery the placenta will then be analysed macroscopically and assessed for several anatomical features. This will be compared with the antenatal complications and perinatal outcomes for the respective twin.",[83,84,29],"Placenta","Monochorionic Twins","RECRUITING","2025-08-08",{"date":88,"type":34},"2025-08-15",{"date":90,"type":34},"2024-12-12",{"date":92,"type":20},"2027-02-01",{"name":94,"class":69},"Birmingham Women's NHS Foundation Trust",{"id":96,"slug":97,"hasResults":11,"nctId":98,"briefTitle":99,"officialTitle":99,"acronym":4,"eligibilityCriteria":100,"healthyVolunteers":11,"sex":17,"minAge":49,"maxAge":4,"enrollmentInfo":101,"targetDuration":4,"studyType":21,"phases":103,"briefSummary":104,"conditions":105,"keywords":4,"overallStatus":85,"whyStopped":4,"lastUpdateSubmitDate":106,"lastUpdatePostDateStruct":107,"startDateStruct":109,"completionDateStruct":111,"leadSponsor":113,"locationsCount":70},"100522150","clinical-feasibility-evaluation-of-the-gentuity-hf-oct-imaging-system-with-vis-m-micro-imaging-catheter-100522150","NCT06078878","Clinical Feasibility Evaluation of the Gentuity HF-OCT Imaging System With Vis-M Micro-Imaging Catheter","Inclusion Criteria:\n\n* Patients who are electively scheduled for either a follow-up cerebral angiogram or a diagnostic angiogram and may be candidates for a neuroendovascular procedure\n* Patients that present with a Modified Rankin Score (mRS) ≤3\n* Patients 18 years of age or older\n* Patients willing and able to provide written informed consent to participate in evaluation\n\nExclusion Criteria:\n\n* Patients with serious concurrent medical conditions including bacteremia or sepsis, acute renal failure at the time of the procedure, and major coagulation system abnormalities that in the opinion of the investigator could significantly increase risk\n* Pregnant\n* Patient has a known hypersensitivity to contrast media\n* Patients undergoing an urgent or emergent neurointerventional procedure\n* Patients that present with a Modified Rankin Score (mRS) ≥4\n* Patients that present with an unresolved spontaneous subarachnoid hemorrhage and\u002For intracranial hemorrhage\n* Participation in another clinical trial of an investigational drug or device\n* Patient has existing Flow Re-Direction Endoluminal Device (FRED®) System",{"count":102,"type":20},30,[23],"This study is a prospective, single arm, unblinded, and open-label study. The study is designed to evaluate the use of the Gentuity Neurovascular Imaging System in patients undergoing elective neurointerventional diagnostic procedures.",[29],"2025-03-25",{"date":108,"type":34},"2025-03-30",{"date":110,"type":34},"2023-02-13",{"date":112,"type":20},"2026-12",{"name":114,"class":115},"Gentuity, LLC","INDUSTRY",{"id":117,"slug":118,"hasResults":11,"nctId":119,"briefTitle":120,"officialTitle":121,"acronym":4,"eligibilityCriteria":122,"healthyVolunteers":11,"sex":78,"minAge":4,"maxAge":4,"enrollmentInfo":123,"targetDuration":4,"studyType":53,"phases":4,"briefSummary":125,"conditions":126,"keywords":4,"overallStatus":85,"whyStopped":4,"lastUpdateSubmitDate":128,"lastUpdatePostDateStruct":129,"startDateStruct":131,"completionDateStruct":133,"leadSponsor":135,"locationsCount":70},"100568250","endoscopic-anatomy-of-the-breast-fascia-system-100568250","NCT06678776","Endoscopic Anatomy of the Breast Fascia System","Endoscopic Anatomy of the Breast Fascia System: A Reverse Development Theory","Inclusion Criteria:\n\n* Breast cancer patients who need mastectomy and patients who need breast reduction during the study period.\n\nExclusion Criteria:\n\n* breast conserving surgery",{"count":124,"type":20},184,"This study will focus on two key theories: the development theory of the breast fascia system and the reverse development theory. The research findings indicate that breast development generally follows a growth pattern from anterior to posterior, and from central to peripheral regions. However, an intriguing phenomenon contradicting this developmental process was discovered through endoscopic mastectomy, which has not been previously discussed. Based on the aforementioned theoretical analysis, this study includes patients who underwent endoscopic and reduction mammaplasty in the Department of Breast Surgery in the Sixth Affiliated Hospital of Sun Yat-sen University. The investigators proposed the following research framework: firstly, comprehensively understanding the structure of the breast fascia and the sequence of breast development through endoscope and existing research; secondly, exploring the relationship between breast fascia development and surgical processes by repeatedly observing surgical videos of endoscopic mastectomy and reduction mammaplasty; lastly, proposing a reverse development theory for breast fascia based on these theories in order to provide standardized and procedural guidance for breast surgeons.",[127,29],"Breast Disease","2024-11-06",{"date":130,"type":34},"2024-11-07",{"date":132,"type":34},"2019-06-01",{"date":134,"type":20},"2024-12-30",{"name":136,"class":41},"Haiyan Li"]