[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"perioperative-management\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:perioperative-management":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,40,68,96],{"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":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":29,"lastUpdatePostDateStruct":30,"startDateStruct":33,"completionDateStruct":35,"leadSponsor":37,"locationsCount":4},"100641179","metabolic-and-clinical-effects-of-hyperchloremia-during-holep-surgery-100641179",false,"NCT07655830","Metabolic and Clinical Effects of Hyperchloremia During HoLEP Surgery.","Evaluation of the Metabolic and Clinical Effects of Intraoperative Hyperchloremia in Holmium Laser Enucleation of Prostate (HoLEP) Surgery.","Inclusion Criteria:\n\n* Patients scheduled for elective HoLEP surgery.\n* Patients providing written informed consent\n\nExclusion Criteria:\n\n* Preoperative metabolic acidosis.\n* Advanced renal failure.\n* Emergency surgery.\n* Missing data.",true,"MALE","18 Years",{"count":20,"type":21},45,"ESTIMATED","OBSERVATIONAL","This study aims to evaluate the changes between preoperative and postoperative serum chloride levels in patients undergoing HoLEP surgery and to investigate the metabolic and clinical effects of this change. The study is observational, and no additional interventions will be performed.",[25,26,27],"HoLEP (Holmium Laser Enucleation of Prostate)","Hyperchloremia","Perioperative Management","NOT_YET_RECRUITING","2026-06-13",{"date":31,"type":32},"2026-06-18","ACTUAL",{"date":34,"type":21},"2026-07-04",{"date":36,"type":21},"2026-09-30",{"name":38,"class":39},"Ankara City Hospital Bilkent","OTHER",{"id":41,"slug":42,"hasResults":11,"nctId":43,"briefTitle":44,"officialTitle":44,"acronym":45,"eligibilityCriteria":46,"healthyVolunteers":11,"sex":47,"minAge":18,"maxAge":4,"enrollmentInfo":48,"targetDuration":4,"studyType":50,"phases":51,"briefSummary":53,"conditions":54,"keywords":4,"overallStatus":57,"whyStopped":4,"lastUpdateSubmitDate":58,"lastUpdatePostDateStruct":59,"startDateStruct":61,"completionDateStruct":63,"leadSponsor":65,"locationsCount":67},"100619021","preoperative-hemodialysis-timing-in-patients-with-end-stage-kidney-disease-the-pod-eskd-pilot-trial-100619021","NCT07339202","Preoperative Hemodialysis Timing in Patients With End-Stage Kidney Disease: The POD-ESKD Pilot Trial","POD-ESKD","Inclusion Criteria:\n\n1. Patient is willing to comply with all study procedures for the duration of the study\n2. Patient has a diagnosis of ESKD\n3. Patient initiated hemodialysis at least 90 days prior to the planned surgical procedure\n4. Patient is treated with a stable hemodialysis schedule, defined as an average of 2.5- 3.5 hemodialysis sessions per week in the preceding 4 weeks prior to surgery\n5. Patient is scheduled to undergo nonemergent surgical procedures in the Stanford Health Care system. This includes (but is not limited to):\n\n   * Fistula or graft creation, revision, or removal\n   * Fistulogram\n   * Peritoneal dialysis catheter placement or revision\n   * Lower extremity angiogram (including femoral and iliac vessels)\n   * Lower extremity bypass (including femoral and iliac vessels)\n   * Lower extremity amputation\n   * Lower extremity endarterectomy (including femoral and iliac vessels) Of note, this list of procedures is not exhaustive and other procedures may be considered that meet inclusion criteria and no exclusion criteria, in consultation with the treatment teams involved.\n\nExclusion Criteria:\n\n1. Patient is pregnant\n2. Patient is a prisoner\n3. Patient is \\\u003C 18 years old\n4. The treating clinicians determine that the patient's clinical condition necessitate a specific approach to surgical scheduling or preoperative hemodialysis","ALL",{"count":49,"type":21},30,"INTERVENTIONAL",[52],"NA","The goal of this clinical trial is to evaluate the feasibility of two different preoperative hemodialysis schedules for people with end-stage kidney disease (ESKD) who undergo surgical procedures. The main questions it aims to answer are:\n\nIs it feasible to randomize participants with ESKD undergoing nonemergent surgical procedures to same-day hemodialysis versus no same-day hemodialysis?\n\nIs it safe to randomize participants with ESKD undergoing nonemergent surgical procedures to same-day hemodialysis versus no same-day hemodialysis?\n\nResearchers will compare the two hemodialysis schedules to see if the scheduling and safety profiles are the same.\n\nParticipants will:\n\nAnswer questions about their health up to 4 weeks before and 4 weeks after the surgical procedure.\n\nReceive hemodialysis on the day of the surgical procedure or not, depending on the study treatment assignment.",[27,55,56],"End Stage Kidney Disease (ESRD)","Hemodialysis","RECRUITING","2026-06-08",{"date":60,"type":32},"2026-06-11",{"date":62,"type":32},"2026-05-27",{"date":64,"type":21},"2027-10-15",{"name":66,"class":39},"Stanford University",1,{"id":69,"slug":70,"hasResults":11,"nctId":71,"briefTitle":72,"officialTitle":72,"acronym":4,"eligibilityCriteria":73,"healthyVolunteers":11,"sex":47,"minAge":18,"maxAge":74,"enrollmentInfo":75,"targetDuration":4,"studyType":50,"phases":77,"briefSummary":78,"conditions":79,"keywords":83,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":87,"lastUpdatePostDateStruct":88,"startDateStruct":90,"completionDateStruct":92,"leadSponsor":94,"locationsCount":4},"100616780","the-construction-and-clinical-application-of-an-integrated-perioperative-management-system-for-lung-cancer-based-on-wearable-devices-and-intelligent-platforms-100616780","NCT07310056","The Construction and Clinical Application of an Integrated Perioperative Management System for Lung Cancer Based on Wearable Devices and Intelligent Platforms","Inclusion Criteria:\n\nAge ≥18 years and ≤85 years\n\nPathologically confirmed primary non-small cell lung cancer (NSCLC)\n\nScheduled to undergo elective curative-intent thoracoscopic lobectomy or segmentectomy\n\nPostoperative clinical condition is stable and judged by investigators to be suitable for discharge within 2-7 days after surgery\n\nAble to independently operate a smartphone and wearable device, or able to do so with caregiver assistance\n\nWilling to comply with study procedures and follow-up requirements\n\nProvided written informed consent prior to participation\n\nExclusion Criteria:\n\nPreoperative long-term home oxygen therapy or severe resting respiratory failure\n\nPresence of severe or uncontrolled cardiopulmonary disease, cerebrovascular disease, hepatic insufficiency, or renal insufficiency\n\nSevere comorbid conditions that significantly limit physical activity or adherence to rehabilitation\n\nKnown or suspected allergy to materials used in wearable devices or medical adhesives\n\nSevere postoperative complications requiring reoperation or prolonged mechanical ventilation\n\nOccurrence of serious adverse events during the six-minute walk test that prevent continuation of the study\n\nAny other condition that, in the judgment of the investigators, makes the participant unsuitable for study participation","85 Years",{"count":76,"type":21},126,[52],"This study aims to develop and evaluate an integrated perioperative management system based on wearable devices and a digital rehabilitation platform for patients with non-small cell lung cancer (NSCLC) undergoing thoracic surgery. By combining preoperative functional assessment using the six-minute walk test (6MWT), continuous perioperative physiological monitoring, and structured postoperative home-based digital rehabilitation, this randomized controlled trial will investigate whether the wearable-based digital management model improves short-term postoperative pulmonary function, functional recovery, and clinical outcomes compared with standard perioperative care.",[80,81,82,27],"Non-Small Cell Lung Cancer (NSCLC)","Rehabilitation","Thoracic Surgery",[84,85,86,27,81],"Non-Small Cell Lung Cancer","Lung Cancer Surgery","Wearable Devices","2025-12-29",{"date":89,"type":32},"2025-12-30",{"date":91,"type":21},"2026-01-01",{"date":93,"type":21},"2026-12-01",{"name":95,"class":39},"West China Hospital",{"id":97,"slug":98,"hasResults":11,"nctId":99,"briefTitle":100,"officialTitle":101,"acronym":4,"eligibilityCriteria":102,"healthyVolunteers":11,"sex":47,"minAge":4,"maxAge":4,"enrollmentInfo":103,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":105,"conditions":106,"keywords":4,"overallStatus":57,"whyStopped":4,"lastUpdateSubmitDate":110,"lastUpdatePostDateStruct":111,"startDateStruct":113,"completionDateStruct":115,"leadSponsor":117,"locationsCount":67},"100574996","the-application-of-eye-tracking-technology-in-perioperative-management-and-education-100574996","NCT06766539","The Application of Eye-Tracking Technology in Perioperative Management and Education","The Application of Eye-Tracking Technology in Perioperative Management and Education: a Prospective Observational Study","Inclusion Criteria:\n\n* Anesthesiologists, including senior physicians and junior doctors.\n* Medical students undergoing perioperative management training.\n\nExclusion Criteria:\n\n* Individuals with ophthalmological conditions that affect eye movement function.\n* Participants who fail to complete the full experimental protocol.",{"count":104,"type":21},300,"The goal of this observational study is to explore the value of eye-tracking technology in perioperative management and teaching. The study aims to understand how eye-tracking can help analyze the attention distribution of clinicians during perioperative procedures and optimize workflows for improved safety and teaching outcomes.\n\nThe main questions it seeks to answer are:\n\nHow does eye-tracking technology reveal the focus distribution patterns of experienced and novice clinicians in perioperative scenarios? Can visualizing expert clinicians' eye movement patterns improve the learning outcomes and operational skills of medical students?\n\nParticipants include anesthesiologists and medical students involved in perioperative management training. Eye-tracking data, such as fixation duration, fixation count, and heatmaps, will be collected during surgical and training scenarios. The study will analyze correlations between attention distribution and operational performance. This research will provide insights into optimizing perioperative safety and revolutionizing medical education using objective attention data.",[107,108,27,109],"Eye-tracking Technology","Medical Education","Attention Distribution","2025-01-05",{"date":112,"type":32},"2025-01-09",{"date":114,"type":32},"2024-12-01",{"date":116,"type":21},"2025-12",{"name":118,"class":39},"Second Affiliated Hospital, School of Medicine, Zhejiang University"]