[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"oxygen\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:oxygen":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,46],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":22,"studyType":23,"phases":4,"briefSummary":24,"conditions":25,"keywords":28,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":45},"100630411","oxygenation-in-posterior-stabilization-surgery-100630411",false,"NCT07487324","Oxygenation in Posterior Stabilization Surgery","Factors Determining Oxygenation in Posterior Stabilization Surgery: The Role of Positioning and Mechanical Ventilation Parameters","Inclusion Criteria:\n\nPatients aged 18 to 75 years Patients classified as ASA physical status I, II, or III according to the American Society of Anesthesiologists Patients undergoing posterior stabilization surgery Patients who voluntarily agreed to participate in the study Patients with a body mass index (BMI) \\\u003C35 kg\u002Fm² Patients followed with a standard mechanical ventilation procedure\n\nExclusion Criteria:\n\n* \\- ASA 4 olarak değerlendirilenler\n* Anestezik ajan alerjisi olanlar\n* Kanama diatezi bozukluğu olanlar\n* Cerrahi süresi 3 saatin üstünde olanlar\n* Bilinen ileri akciğer hastalığı olanlar (intertisyel akciğer hastalığı, ileri düzey KOAH, ileri düzey astım vb)\n* VKI≥35 olanlar\n* Obstrüktif uyku apne sendromu tanısı olanlar\n* Toraks deformitesi olanlar\n* Ciddi kalp yetmezliği öyküsü olanlar (EF\\\u003C30)\n* Şiddetli anemi öyküsü olanlar (Hg\\\u003C8 mg\u002Fdl)\n* Cerrahi operasyon sırasında kan transfüzyonu ihtiyacı olan hastalar","ALL","18 Years","80 Years",{"count":20,"type":21},50,"ESTIMATED","1 Day","OBSERVATIONAL","This study aims to evaluate the effects of prone positioning on oxygenation, ventilation, and hemodynamic parameters in patients undergoing posterior stabilization surgery under general anesthesia. By comparing routine anesthesia and monitoring data obtained in the supine and prone positions, the study seeks to determine how positional changes influence respiratory mechanics and perioperative physiological stability.",[26,27],"Oxygen","Oxygen Saturation",[29,30,31,32],"oxygenation","Posterior Stabilization Surgery","Mechanical Ventilation Parameters","optic nerve sheath diamater","NOT_YET_RECRUITING","2026-03-17",{"date":36,"type":37},"2026-03-23","ACTUAL",{"date":39,"type":21},"2026-04-01",{"date":41,"type":21},"2026-11-15",{"name":43,"class":44},"Sakarya University","OTHER",1,{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":4,"eligibilityCriteria":52,"healthyVolunteers":53,"sex":16,"minAge":4,"maxAge":4,"enrollmentInfo":54,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":56,"conditions":57,"keywords":4,"overallStatus":61,"whyStopped":4,"lastUpdateSubmitDate":62,"lastUpdatePostDateStruct":63,"startDateStruct":65,"completionDateStruct":67,"leadSponsor":69,"locationsCount":72},"100544685","project-mountain---comparing-spo2-and-sao2-for-accuracy-100544685","NCT06372106","Project Mountain - Comparing SpO2 and SaO2 for Accuracy","Philips FAST picoSAT Convenience Sampling for Clinical Performance in Neonate, Infant, and Pediatric Patients","Inclusion Criteria:\n\n* Subject aged 18 years or older or parent\u002Flegal guardian of subject aged less than 18 years, willing and able to understand and provide written informed consent\u002Fassent.\n* Weight and\u002For age within intended use of at least one SpO2 sensor under test at time of enrollment.\n* Willing and able to wear study devices in addition to SoC devices and during SoC procedures.\n* In-patient within a neonatal or pediatric intensive care unit (e.g. NICU, PICU, PCICU).\n* Has arterial access and ability to have arterial blood samples drawn as part of their SoC and analyzed by CO-Oximetry.\n\nExclusion Criteria:\n\n* Known pregnancy or lactating females (self-reported)\n* Injury, wounds, physical malformation, hyperkeratosis, or compromised\u002Fnon-intact skin at sensor application site (i.e. fingers, toes, hands, feet, ears, nasal ala). Note: Certain malformations may be allowed if determined it would not affect application of sensor with the pulse oximetry system.\n* Self-reported severe contact allergies to standard adhesives or other materials found in pulse oximetry sensors. Note: Subject may be considered eligible if subject can wear non-adhesive sensor.\n* Unwillingness or inability to remove nail polish or artificial nails from sensor application site.\n* Nail fungus on sensor application site.\n* Wearing and unable to remove jewelry from sensor application site.\n* Dye injection within 48 hours of enrollment.\n* Known dysfunctional hemoglobin levels (COHb \\>3%, MetHb \\>2%, and ctHb \\\u003C10g\u002Fdl)\n* Undergoing phototherapy for neonatal hyperbilirubinemia during arterial blood sampling",true,{"count":55,"type":21},560,"The main goal of this study is to look at the performance of the neonatal, infant, and pediatric Philips SpO2 sensors with the Philips FAST Pulse Oximetry technology. Oxygen saturation measurements (SpO2) will be obtained via pulse oximetry and invasive arterial oxygen measurements (SaO2) will be obtained via arterial blood samples as part of your clinical care and assessed by co-oximetry. The study will aim to enroll a diverse population to help us understand the impact of skin pigmentation.",[58,59,26,60],"SpO2","Nasal Alar Collapse, Bilateral","Measurement","RECRUITING","2025-04-01",{"date":64,"type":37},"2025-04-02",{"date":66,"type":37},"2024-04-04",{"date":68,"type":21},"2025-12",{"name":70,"class":71},"Philips Clinical & Medical Affairs Global","INDUSTRY",5]