[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"fetal-conditions\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:fetal-conditions":24},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,40,73],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":4,"maxAge":4,"enrollmentInfo":16,"targetDuration":4,"studyType":19,"phases":20,"briefSummary":22,"conditions":23,"keywords":25,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":28,"lastUpdatePostDateStruct":29,"startDateStruct":32,"completionDateStruct":34,"leadSponsor":36,"locationsCount":39},"100309003","the-value-of-advanced-imaging-sequences-for-fetal-mri-in-clinical-practice-100309003",false,"NCT03302663","The Value of Advanced Imaging Sequences for Fetal MRI in Clinical Practice","Inclusion Criteria:\n\n* Pregnant women who are attending the fetal medicine clinic and are asked to consider an MRI scan to provide information to help manage the current pregnancy.\n* Pregnant women requesting a termination of pregnancy who will allow us to do fetal MRI at 3T prior to the termination.\n\nExclusion Criteria:\n\n* Contraindication to MRI\n* Severe claustrophobia","FEMALE",{"count":17,"type":18},150,"ESTIMATED","INTERVENTIONAL",[21],"NA","This project is split into 4 sections:\n\n1. Can improvements be made in the Magnetic resonance imaging sequences used to image the fetus in order to improve diagnostic accuracy?\n2. Does 3T improve the quality and diagnostic value of fetal MRI when compared to 1.5T\n3. Can fetal MRI be used to image the fetal heart?\n4. Can fetal MRI be used to image the fetal Bones?",[24],"Fetal Conditions",[26],"Fetal bone heart abnormality","RECRUITING","2025-05-30",{"date":30,"type":31},"2025-06-04","ACTUAL",{"date":33,"type":31},"2013-08-01",{"date":35,"type":18},"2025-12-31",{"name":37,"class":38},"Sheffield Teaching Hospitals NHS Foundation Trust","OTHER",1,{"id":41,"slug":42,"hasResults":11,"nctId":43,"briefTitle":44,"officialTitle":45,"acronym":4,"eligibilityCriteria":46,"healthyVolunteers":47,"sex":15,"minAge":48,"maxAge":49,"enrollmentInfo":50,"targetDuration":4,"studyType":19,"phases":52,"briefSummary":53,"conditions":54,"keywords":57,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":64,"lastUpdatePostDateStruct":65,"startDateStruct":67,"completionDateStruct":69,"leadSponsor":71,"locationsCount":39},"100539297","the-effect-of-stress-ball-intervention-during-non-stress-test-on-anxiety-and-fetal-well-being-in-high-risk-pregnancy-100539297","NCT06302010","The Effect of Stress Ball Intervention During Non-Stress Test on Anxiety and Fetal Well-Being in High-Risk Pregnancy","The Effect of Stress Ball Intervention During Non-Stress Test on Anxiety and Fetal Well-Being in Women With High-risk Pregnancy: A Randomized Controlled Study","Inclusion Criteria:\n\n* Volunteering to participate in the research,\n* Being over 18 years of age,\n* Having a medically diagnosed risky condition during pregnancy (diabetes, hypertension, the threat of premature birth, eclampsia, etc.)\n* Compliance with at least one of the criteria in the \"Ministry of Health Pregnancy Risk Assessment Form\" in the evaluation of \"Current Pregnancy\" (Table 1)\n* Being at or above the 32nd week of pregnancy,\n* Having a single living fetus,\n* Having eaten at least two hours before the NST procedure,\n* Not having smoked or consumed alcohol at least two hours before the NST procedure,\n* Knowing how to read and write Turkish.\n\nExclusion Criteria:\n\n* Deceleration or uterine contraction during NST,\n* Presence of cardiovascular disease in the fetus,\n* Presence of fetal distress,\n* Presence of fetal anomaly,\n* According to the physician, urgent intervention is needed,\n* Having a diagnosed psychiatric disease,\n* Having a visual, hearing, speaking, physical or mental disability.",true,"18 Years","45 Years",{"count":51,"type":18},86,[21],"This research will be conducted to determine the effect of stress ball intervention during NST on anxiety and fetal well-being in high-risk pregnant women. Women with high-risk pregnancies randomly assigned to intervention (n=43) and control (n=43) groups at a state and a faculty hospital in Turkey will be included in the study. Pregnant women in the intervention group will be told to squeeze and release the ball once after counting to three, to inhale each time they press the ball, to exhale when they relax their grip and to focus only on the ball. Pregnant women will be instructed to continue this practice throughout the NST procedure (approximately 20 minutes). Pregnant women in the control group will not receive any intervention other than routine hospital care during the NST procedure. Data on anxiety and fetal well-being outcomes will be collected before and after NST.",[55,24,56],"Anxiety","Pregnancy Related",[58,59,60,61,62,63],"anxiety","fetal well-being","high-risk pregnant women","Non stres test","stress ball","nurse","2024-12-28",{"date":66,"type":31},"2024-12-31",{"date":68,"type":31},"2024-03-13",{"date":70,"type":18},"2025-08-31",{"name":72,"class":38},"Hümeyra TÜLEK DENİZ",{"id":74,"slug":75,"hasResults":11,"nctId":76,"briefTitle":77,"officialTitle":77,"acronym":4,"eligibilityCriteria":78,"healthyVolunteers":11,"sex":15,"minAge":48,"maxAge":49,"enrollmentInfo":79,"targetDuration":4,"studyType":19,"phases":81,"briefSummary":82,"conditions":83,"keywords":92,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":96,"lastUpdatePostDateStruct":97,"startDateStruct":99,"completionDateStruct":101,"leadSponsor":103,"locationsCount":39},"100520443","a-prospective-study-on-the-role-of-karl-storz-curved-and-straight-fetoscopes-11508aak-and-11506aak-for-fetoscopic-intrauterine-procedures-100520443","NCT06056635","A Prospective Study on the Role of Karl Storz Curved and Straight Fetoscopes (11508AAK and 11506AAK) for Fetoscopic Intrauterine Procedures","Inclusion Criteria:\n\n* Pregnant patient with a condition requiring in-utero surgery\n* Patient must be eligible for anesthesia\n* Patient and father of the fetus (if available) are able to provide signed informed consent\n\nExclusion Criteria:\n\n* Allergy or previous adverse reaction to any ancillary medication specified in this protocol that has no alternative\n* Preterm labor, preeclampsia, or uterine anomaly (e.g., large fibroid tumor) in the index pregnancy\n* Suspicion of major recognized congenital syndrome on ultrasound or MRI that is not compatible with postnatal life\n* Pre-pregnancy maternal BMI greater than 40\n* High risk for fetal hemophilia\n* Fetal aneuploidy or variants of known significance if an amniocentesis was performed\n* Contraindication to abdominal surgery or fetoscopic surgery",{"count":80,"type":18},50,[21],"In this research study, the investigators want to learn more about the role of new innovative surgical devices, the Karl Storz Curved and Straight Fetoscopes for in-utero surgery. A fetoscope is like a small telescope that can see inside of the uterus (womb) during minimally invasive surgery. The curved scope is used for patients with an anterior placenta (front of uterus), while the straight scope is used for patients with a posterior placenta (back of uterus). The scopes will be used to assist in procedures involving fetoscopic laser photocoagulation (FLP), which is a minimally invasive surgery that uses a small camera (fetoscope) to locate abnormal blood vessel connections in the placenta and seal them off using laser energy. These fetoscopes will be utilized in the diagnosis and management of various fetal conditions that can arise during pregnancy. Outcome data will be reported in a descriptive statistical analysis. The investigators will assess the surgical outcomes, short and long-term morbidity, complications, and gestational age of participants in order to evaluate the benefit of using these devices.",[24,84,56,85,86,87,88,89,90,91],"Maternal; Procedure","Twin to Twin Transfusion Syndrome","In Utero Procedure Affecting Fetus or Newborn","Chorion; Abnormal","Twin Reversal Arterial Perfusion Syndrome","Twin Monochorionic Monoamniotic Placenta","Chorioangioma","Vasa Previa",[93,94,95],"Fetoscope","Fetoscopic Laser Ablation","Diagnostic Fetoscopy","2024-09-24",{"date":98,"type":31},"2024-09-25",{"date":100,"type":31},"2024-08-15",{"date":102,"type":18},"2027-05-01",{"name":104,"class":38},"Boston Children's Hospital"]