[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"The Chaim Sheba Medical Center\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":100},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,48,79],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":29,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"100115485","phase-4-the-psychiatric-and-cognitive-phenotypes-in-velocardiofacial-syndrome-100115485",false,"NCT00768820","The Psychiatric and Cognitive Phenotypes in Velocardiofacial Syndrome","The Psychiatric and Cognitive Phenotypes in Velocardiofacial Syndrome (VCFS), Williams Syndrome (WS)and Fragile X Syndrome Characterization, Treatment and Examining the Connection to Developmental and Molecular Factors","VCFS","Inclusion Criteria:\n\n* chromosomal deletion proven by FISH examination\n\nExclusion Criteria:","ALL",{"count":19,"type":20},400,"ESTIMATED","INTERVENTIONAL",[23],"PHASE4","The purpose of this study is to investigate the Psychiatric and Cognitive Phenotypes in Velocardiofacial Syndrome (VCFS), Williams Syndrome (WS)and Fragile X Syndrome Characterization, Treatment and Examining the Connection to Developmental and Molecular Factors",[26,27,28],"Velocardiofacial Syndrome","Williams Syndrome","Fragile X Syndrome",[30,31,32,33,34],"Velocardiofacial syndrome","Williams syndrome","fragile X syndrome","cognitive phenotype","psychiatric phenotype","RECRUITING","2026-03-17",{"date":38,"type":39},"2026-03-18","ACTUAL",{"date":41,"type":4},"2001-05",{"date":43,"type":20},"2027-08",{"name":45,"class":46},"The Chaim Sheba Medical Center","OTHER",1,{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":4,"eligibilityCriteria":54,"healthyVolunteers":11,"sex":55,"minAge":56,"maxAge":4,"enrollmentInfo":57,"targetDuration":59,"studyType":60,"phases":4,"briefSummary":61,"conditions":62,"keywords":66,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":71,"lastUpdatePostDateStruct":72,"startDateStruct":74,"completionDateStruct":76,"leadSponsor":78,"locationsCount":4},"100613855","maternal-and-fetal-clinical-significance-of-hypotension-following-labor-epidural-analgesia-100613855","NCT07272018","Maternal and Fetal Clinical Significance of Hypotension Following Labor Epidural Analgesia","Incidence and Clinical Significance of Maternal Hypotension After Labor Epidural Analgesia and Its Effects on Fetal Well-Being","Inclusion Criteria:\n\n* 18 years of age or older\n* 37 weeks pregnant or more (term pregnancy)\n* in labor and choose to receive an epidural for pain relief\n* giving birth at Sheba Medical Center\n\nExclusion Criteria:\n\n* patients with a heart condition that requires special blood pressure management\n* medical conditions that prevent safe monitoring of blood pressure\n* missing or incomplete medical record data needed for the study\n* patient who do not receive an epidural during labor","FEMALE","18 Years",{"count":58,"type":20},480,"7 Days","OBSERVATIONAL","The goal of this study is to learn how often blood pressure drops after an epidural for labor and how these drops may affect the parent and the baby. The study focuses on adults who give birth at term and choose to receive an epidural for pain relief.\n\nThe main questions the study aims to answer are:\n\nHow often does maternal blood pressure fall within 30 minutes after the epidural? When blood pressure falls, how often do participants need treatments such as fluids or medicines that raise blood pressure? Do changes in the baby's heart rate happen during this time, and do they need treatment? Are certain parent or labor factors linked to a higher chance of blood pressure drops? How often does an urgent cesarean delivery happen because of maternal low blood pressure or concerning fetal heart rate changes soon after the epidural?\n\nParticipants will not be asked to do anything different from usual care. Researchers will:\n\nReview routine vital signs recorded before and after the epidural Review treatments given, such as IV fluids or blood-pressure-raising medicines Review the baby's heart-rate monitoring Record delivery information, including whether an urgent cesarean was needed This study does not change clinical care in any way. It uses information already collected during standard labor and delivery.",[63,64,65],"Maternal Hypotension","Labor Epidural Analgesia","Fetal Heart Rate Abnormalities",[64,67,63,65,68,69],"Post-Epidural Hypotension","Non-Reassuring Fetal Heart Rate","Obstetric Anesthesia","NOT_YET_RECRUITING","2025-11-26",{"date":73,"type":39},"2025-12-09",{"date":75,"type":20},"2025-12",{"date":77,"type":20},"2026-03",{"name":45,"class":46},{"id":80,"slug":81,"hasResults":11,"nctId":82,"briefTitle":83,"officialTitle":84,"acronym":4,"eligibilityCriteria":85,"healthyVolunteers":11,"sex":55,"minAge":56,"maxAge":4,"enrollmentInfo":86,"targetDuration":4,"studyType":60,"phases":4,"briefSummary":88,"conditions":89,"keywords":4,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":92,"lastUpdatePostDateStruct":93,"startDateStruct":95,"completionDateStruct":97,"leadSponsor":99,"locationsCount":4},"100577817","ultrasound-assessment-of-gastric-volume-in-high-risk-pregnant-women-at-term-100577817","NCT06803225","Ultrasound Assessment of Gastric Volume in High-Risk Pregnant Women At Term","ULTRASOUND ASSESSMENT of GASTRIC CONTENT in FASTED PREGNANT WOMEN: PROSPECTIVE OBSERVATIONAL STUDY","Inclusion Criteria:\n\n1. Non-labouring pregnant women at 3rd trimester (≥ 28 weeks)\n2. 18 years or older.\n3. ASA physical status I-III\n4. Hospitilized in High Risk Pregnancy Department\n5. Ability to understand the rationale of the study assessments and provide signed informed consent.\n6. Written informed consent\n\nExclusion Criteria:\n\n1. Patients with American Society of Anesthesiology (ASA) physical status class IV.\n2. Patient age \\\u003C 18 years\n3. Pregnant patients with upper gastrointestinal (GI) disease and pathology.\n4. History of upper GI tract surgical procedures.\n5. History of medications that affect gastrointestinal motility.\n6. Inability to understand the rationale of the study assessments and provide signed informed consent.",{"count":87,"type":20},500,"The risk of pulmonary aspiration of gastric contents remains a significant risk during anesthesia, especially in pregnant women, as they may often require surgery without having observed appropriate fasting. A bedside ultrasound assessment of the status of the gastric content would be of great value for the clinician.\n\nThis prospective observational study aimed to (1) qualitatively and quantitatively describe the sonographic appearance of the gastric antrum in fasted high-risk pregnant women during the third trimester and (2) evaluate the relationship between demographic and clinical variables and the gastric antral cross-sectional area (CSA).",[90,91],"Pregnancy","Respiratory Aspiration of Gastric Content","2025-01-27",{"date":94,"type":39},"2025-01-31",{"date":96,"type":20},"2025-03-01",{"date":98,"type":20},"2025-11-01",{"name":45,"class":46},""]