[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"monitoring-physiologic\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:monitoring-physiologic":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,50,74],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":23,"conditions":24,"keywords":30,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":38,"lastUpdatePostDateStruct":39,"startDateStruct":42,"completionDateStruct":44,"leadSponsor":46,"locationsCount":49},"100613000","paired-comparison-of-svv-and-pvi-accuracy-100613000",false,"NCT07260890","Paired Comparison of SVV and PVI Accuracy","Diagnostic Accuracy of Stroke Volume Variation (SVV) vs Pleth Variability Index (PVI) for Predicting Fluid Responsiveness in Laparoscopic Major Abdominal Surgery-A Prospective, Paired, Cohort Study","Inclusion Criteria:\n\n* Age ≥18 years\n* ASA physical status I-III\n* Elective laparoscopic major abdominal surgery under general anesthesia\n* Arterial line in place for clinical care\n* Able to provide informed consent\n* Arterial and plethysmographic waveforms adequate for measurement\n\nExclusion Criteria:\n\n* linically significant arrhythmia (e.g., atrial fibrillation with irregular R-R)\n* Severe valvular heart disease or intracardiac shunt\n* Pregnancy\n* Severe right-heart failure or condition where a fluid bolus is unsafe\n* Ongoing hemodynamic instability requiring rapid vasoactive titration at assessment\n* Persistently unreliable arterial\u002Fpleth signals despite optimization\n* Any situation the anesthesiologist judges that the fluid challenge is unsafe",true,"ALL","19 Years",{"count":20,"type":21},300,"ESTIMATED","OBSERVATIONAL","This study will compare two operating-room monitors-stroke volume variation (SVV, from the arterial line) and the Pleth Variability Index (PVI, from the pulse oximeter)-to see which one more accurately predicts whether giving a small fluid bolus will improve the heart's pumping during laparoscopic major abdominal surgery. Adults having elective surgery under general anesthesia will receive two small, timed 250-mL crystalloid infusions as part of routine care (one before and one after creation of the pneumoperitoneum). The research team will record SVV and PVI values just before and three minutes after each infusion while keeping these readings hidden from the clinicians so that usual care is not changed. No experimental drugs or devices are used. The main goal is to learn which index better identifies \"fluid responsiveness,\" so future care can be safer and more consistent. Potential risks are minimal and relate to the small fluid boluses (temporary changes in blood pressure or heart rate); the test stops if the anesthesiologist has any safety concerns. There is no direct benefit to participants, but results may help guide fluid therapy for similar patients in the future. The study is being conducted at a single academic hospital in the Republic of Korea and plans to enroll about 300 adults.",[25,26,27,28,29],"Perioperative Care","Fluid Therapy","Monitoring, Physiologic","Hemodynamics","Laparoscopy",[31,32,33,34,35,36],"stroke volume variation; SVV","Pleth Variability Index; PVI","fluid responsiveness","goal-directed fluid therapy; GDFT","pneumoperitoneum","diagnostic accuracy; ROC; AUROC","RECRUITING","2026-06-24",{"date":40,"type":41},"2026-06-26","ACTUAL",{"date":43,"type":21},"2026-07-01",{"date":45,"type":21},"2026-08-30",{"name":47,"class":48},"Wonkwang University Hospital","OTHER",1,{"id":51,"slug":52,"hasResults":11,"nctId":53,"briefTitle":54,"officialTitle":54,"acronym":4,"eligibilityCriteria":55,"healthyVolunteers":11,"sex":17,"minAge":56,"maxAge":57,"enrollmentInfo":58,"targetDuration":4,"studyType":60,"phases":61,"briefSummary":63,"conditions":64,"keywords":4,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":65,"lastUpdatePostDateStruct":66,"startDateStruct":68,"completionDateStruct":70,"leadSponsor":72,"locationsCount":49},"100438993","day-case-colectomy-optimizing-short-stay-surgery-100438993","NCT04996511","Day Case Colectomy: Optimizing Short Stay-surgery.","Inclusion Criteria:\n\n• Colorectal resection for any pathology\n\nExclusion Criteria:\n\n• Arrhytmias likely to cause problems with HRV measurements","18 Years","100 Years",{"count":59,"type":21},30,"INTERVENTIONAL",[62],"NA","HRV measurement of patients recovering from laparoscopic colorectal resection for any pathology.",[27],"2026-04-21",{"date":67,"type":41},"2026-04-22",{"date":69,"type":41},"2020-01-01",{"date":71,"type":21},"2027-12-31",{"name":73,"class":48},"Joint Authority for Päijät-Häme Social and Health Care",{"id":75,"slug":76,"hasResults":11,"nctId":77,"briefTitle":78,"officialTitle":78,"acronym":4,"eligibilityCriteria":79,"healthyVolunteers":11,"sex":17,"minAge":56,"maxAge":4,"enrollmentInfo":80,"targetDuration":4,"studyType":60,"phases":82,"briefSummary":83,"conditions":84,"keywords":4,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":88,"lastUpdatePostDateStruct":89,"startDateStruct":91,"completionDateStruct":93,"leadSponsor":95,"locationsCount":49},"100596949","non-invasive-blood-pressure-monitoring-in-icu-patients-using-the-dare-device-100596949","NCT07052123","Non-Invasive Blood Pressure Monitoring in ICU Patients Using the DARE Device","Inclusion Criteria:\n\n* Adult patients (male or female), aged 18 years or older\n* Admitted to intensive care unit (ICU) or critical care with an expected hospital stay longer than 2 days\n* Equipped with an arterial catheter for invasive blood pressure monitoring\n* Equipped with a urinary catheter for invasive core body temperature monitoring\n\nExclusion Criteria:\n\n* Patients under 18 years old (minors)\n* Known skin allergy to adhesives or silicone, or skin condition preventing adhesive use\n* History of extensive skin pathology (e.g., Lyell syndrome)\n* Patients with therapeutic limitations\n* Patients with active implanted medical devices (e.g., pacemaker, defibrillator)\n* Pregnant or breastfeeding women\n* Patients not affiliated with the French social security system\n* Patients or their legal representatives refusing consent, or unable to understand information and give informed consent\n* Patients under legal guardianship, curatorship, or deprived of liberty",{"count":81,"type":21},2,[62],"This study tests a new non-invasive device called DARE to monitor blood pressure in patients in intensive care. It compares the device's readings to standard invasive methods and also looks at how well it measures other vital signs like temperature, oxygen levels, and heart rhythm. The goal is to improve patient safety and comfort while helping doctors detect problems earlier.",[28,85,86,87,27],"Blood Pressure Monitoring","Intensive Care Units","Critical Illness","2025-06-26",{"date":90,"type":41},"2025-07-04",{"date":92,"type":41},"2025-03-24",{"date":94,"type":21},"2028-03-24",{"name":96,"class":48},"Centre Hospitalier de Saint-Denis"]