[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"perioperative-medicine\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:perioperative-medicine":31},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,5,0,[8,51,88,110,136],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":32,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":39,"lastUpdatePostDateStruct":40,"startDateStruct":43,"completionDateStruct":45,"leadSponsor":47,"locationsCount":50},"100648118","prevention-of-chronic-postsurgical-pain-in-chronic-opioid-users-100648118",false,"NCT07717151","Prevention of Chronic Postsurgical Pain in Chronic Opioid Users:","Ransitional Teleconsultation to Prevent Chronic Postsurgical Pain in Chronic Opioid Users","PRE-OPIOID","Inclusion Criteria:\n\n* Age ≥18 years\n* Elective non-urgent surgery with expected moderate or higher postoperative pain\n* Chronic preoperative opioid use\n* Written informed consent\n* affiliated with a national social security scheme\n\nExclusion Criteria:\n\n* Ambulatory surgery\n* Endoscopic or palliative surgery\n* Patients receiving opioid substitution therapy\n* Non-medical opioid use\n* Intrathecal\u002Fepidural analgesia or implanted neurostimulator\n* Legally protected adults\n* Severe psychiatric or neurodegenerative disorders","ALL","18 Years",{"count":20,"type":21},354,"ESTIMATED","INTERVENTIONAL",[24],"NA","Chronic opioid users undergoing surgery are at increased risk of CPSP, contributing to long-term disability, decreased quality of life, and prolonged opioid exposure. Existing preventive strategies remain limited, and early postoperative monitoring may represent a key opportunity for intervention. Evidence suggests that transitional pain services can improve outcomes by optimizing pain control and reducing long-term opioid consumption, but implementation is heterogeneous and often resource-intensive. Telemedicine offers a scalable alternative, enabling early specialized evaluation and timely therapeutic adjustments while maintaining accessibility. This randomized controlled trial will compare standard postoperative follow-up with standard follow-up plus a specialized teleconsultation performed between postoperative day 15 and 28. The intervention aims to detect insufficiently controlled pain, signs of neuropathic pain, or maladaptive opioid use, and to propose individualized therapeutic adjustments when required.\n\nParticipants will be followed for 6 months. Primary assessment will occur at 3 months to determine CPSP incidence. Secondary assessments will include pain trajectory (intensity, neuropathic features, functional interference), opioid consumption and misuse, quality of life, and a descriptive medico- economic evaluation",[27,28,29,30,31],"Chronic Postsurgical Pain","Chronic Opioid Users","Transitional Pain Service","Postoperative Pain","Perioperative Medicine",[33,34,35,36,37],"Chronic postsurgical pain","chronic opioid users","transitional pain service","postoperative pain","perioperative medicine","RECRUITING","2026-07-16",{"date":41,"type":42},"2026-07-21","ACTUAL",{"date":44,"type":42},"2026-01-14",{"date":46,"type":21},"2029-01",{"name":48,"class":49},"Centre Hospitalier Universitaire, Amiens","OTHER",1,{"id":52,"slug":53,"hasResults":11,"nctId":54,"briefTitle":55,"officialTitle":55,"acronym":56,"eligibilityCriteria":57,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":58,"targetDuration":4,"studyType":60,"phases":4,"briefSummary":61,"conditions":62,"keywords":77,"overallStatus":79,"whyStopped":4,"lastUpdateSubmitDate":80,"lastUpdatePostDateStruct":81,"startDateStruct":83,"completionDateStruct":85,"leadSponsor":86,"locationsCount":50},"100642312","risk-factors-of-atrial-fibrillation-after-cardiac-surgery-100642312","NCT07625033","Risk Factors of Atrial Fibrillation After Cardiac Surgery","PFAS","Inclusion Criteria:\n\n* age \\>18\n* having undergone a scheduled cardiac surgery in the study center\n* having agreed to the reuse of their hospital care data\n\nExclusion Criteria:\n\n* Atrial fibrillation at the admission in hospital.",{"count":59,"type":21},918,"OBSERVATIONAL","Supraventricular arrhythmias complicate more than 40% of cardiac surgeries and are associated with an increased risk of bleeding, stroke, heart failure, and death. Preventing the occurrence of these arrhythmias is a major challenge. This study aims to investigate risk factors and protective factors regarding atrial fibrillation and other iatrogenic cardiac arrhythmias after cardiac surgery, particularly innovative anesthetic strategies such as stellar ganglion blockade which have been recently implemented in our center.",[63,64,65,66,67,68,69,31,70,71,72,73,74,75,76],"Cardiac Surgery","Peri Operative Medicine","Thoracic Surgery","Cardiopulmonary Bypass","Coronary Artery Bypass","Heart Valve Prosthesis Implantation","Aortic Valve Replacement","Preoperative Care","Intraoperative Care","Postoperative Care","Enhanced Recovery After Surgery","Anesthesia","Cardiac Anesthesia","Intensive Care Unit",[78],"Stellar Ganglion Blockade, SGB, cardiac surgery","NOT_YET_RECRUITING","2026-06-23",{"date":82,"type":42},"2026-06-25",{"date":84,"type":21},"2026-07-01",{"date":84,"type":21},{"name":87,"class":49},"Centre Hospitalier Régional Metz-Thionville",{"id":89,"slug":90,"hasResults":11,"nctId":91,"briefTitle":92,"officialTitle":93,"acronym":94,"eligibilityCriteria":95,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":96,"targetDuration":4,"studyType":60,"phases":4,"briefSummary":98,"conditions":99,"keywords":4,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":101,"lastUpdatePostDateStruct":102,"startDateStruct":104,"completionDateStruct":106,"leadSponsor":108,"locationsCount":50},"100517863","preoperative-walking-evaluation-and-postoperative-outcome-100517863","NCT06023069","Preoperative Walking Evaluation and Postoperative Outcome","Preoperative Walking Evaluation and Postoperative Outcome in Non-cardiac Surgery","PREVENT","Inclusion Criteria:\n\nAdult patients (equal to or over 18 years) undergoing elective non-cardiac surgery providing informed consent\n\nExclusion Criteria:\n\nPatients that can not provide informed consent.",{"count":97,"type":21},264,"The hypothesis is that physical activity is associated with a reduced risk of complications and death after surgery.\n\nSelf-reporting of physical activity is prone to be unreliable. In order to obtain a better picture of patients' physical activity, we intend to investigate the association between the average number of steps and postoperative outcomes. Many other objective measures of physical activity are costly and time-consuming to perform; for example, exercise tests, extensive sampling, and longer questionnaires.\n\nThe primary research question is: Do patients with a higher degree of physical activity, measured as the average number of steps recorded on the patient's mobile phone, have a reduced risk of peri\u002Fpostoperative complications and death, measured as Days At Home alive at 30 days (DAH30)?\n\nSecondary research questions include:\n\nIs physical activity, measured as the average number of steps recorded on the patient's mobile phone, linearly linked to DAH30? Is physical activity, measured as the average number of steps recorded on the patient's mobile phone, associated with specific peri\u002Fpostoperative organ impact, such as lung, heart, cerebral, infection, or kidney complications? Is physical activity, measured as the average number of steps recorded on the patient's mobile phone, also linked to long-term outcomes one year after surgery? Is physical activity, measured as the average number of steps recorded on the patient's mobile phone, solely associated with DAH30 and organ complications for specific patient groups in terms of age, comorbidities, and\u002For type of surgery?",[100,31],"General Surgery","2025-08-26",{"date":103,"type":42},"2025-09-03",{"date":105,"type":42},"2023-09-01",{"date":107,"type":21},"2026-12-31",{"name":109,"class":49},"Karolinska Institutet",{"id":111,"slug":112,"hasResults":11,"nctId":113,"briefTitle":114,"officialTitle":115,"acronym":116,"eligibilityCriteria":117,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":118,"targetDuration":4,"studyType":60,"phases":4,"briefSummary":120,"conditions":121,"keywords":124,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":128,"lastUpdatePostDateStruct":129,"startDateStruct":131,"completionDateStruct":133,"leadSponsor":135,"locationsCount":50},"100568218","perioperative-impact-of-physical-activity-on-short--and-long-term-morbidity-and-mortality-100568218","NCT06678360","Perioperative Impact of Physical Activity on Short- and Long-term Morbidity and Mortality","Perioperative Impact After Non-cardiac Surgery of Physical Activity on Short- and Long-term Morbidity and Mortality","PeriopIPA","Inclusion Criteria:\n\nAdult patients (equal to or over 18 years) undergoing elective non-cardiac surgery at the two study sites, Karolinska University Hospital Solna and Karolinska University Hospital Huddinge\n\nExclusion Criteria:\n\nPatients under the age of 18, transplant, day surgery, acute surgery, anesthesia monitoring, brachy therapy and gamma knife interventions. In case of multiple surgeries, only the first will be included.",{"count":119,"type":21},180000,"Over 300 million surgeries are performed globally every year. Complications after surgery - infections, cardiovascular conditions, postoperative pulmonary complications and renal impairment - affect survival and quality of life.\n\nAge and co-morbidity are unmodifiable factors, contributing to increased risk of these perioperative complications. However, a modifiable risk factor is physical activity. This study aims to test if self reported physical activity is associated to lower risk of perioperative morbidity and mortality.",[100,122,31,123],"Perioperative Complication","Physical Inactivity",[125,126,127],"MET-scores","Physical activity","Perioperative mortality","2025-06-02",{"date":130,"type":42},"2025-06-06",{"date":132,"type":42},"2024-11-01",{"date":134,"type":21},"2025-12-01",{"name":109,"class":49},{"id":137,"slug":138,"hasResults":11,"nctId":139,"briefTitle":140,"officialTitle":141,"acronym":142,"eligibilityCriteria":143,"healthyVolunteers":11,"sex":17,"minAge":144,"maxAge":4,"enrollmentInfo":145,"targetDuration":4,"studyType":60,"phases":4,"briefSummary":147,"conditions":148,"keywords":4,"overallStatus":79,"whyStopped":4,"lastUpdateSubmitDate":149,"lastUpdatePostDateStruct":150,"startDateStruct":152,"completionDateStruct":154,"leadSponsor":156,"locationsCount":50},"100496288","aspire-aub-has2-plus-biomarkers-100496288","NCT05742282","ASPIRE (Aub-haS2 Plus bIomaRkErs)","Validation of the AUB-HAS2 Score in a Brazilian Population and Study of the Additional Impact of Biomarkers in Predicting Perioperative Risk","ASPIRE","Inclusion Criteria:\n\n* Age ≥ 40 years, in the preoperative period of non-cardiac procedures, with expected hospitalization for at least 24 hours postoperatively.\n\nExclusion Criteria:\n\n* Refusal to sign the informed consent form.","40 Years",{"count":146,"type":21},2500,"ASPIRE is a prospective, multicenter, observational study that will assess the performance of AUB-HAS2 to predict the occurrence of major adverse cardiovascular events 30-days after a non-cardiac surgery and the additional role of high-sensitivity troponin T and NT-ProBNP biomarkers in the accuracy of different event prediction indexes after non-cardiac procedures.",[31],"2025-05-15",{"date":151,"type":42},"2025-05-20",{"date":153,"type":21},"2025-06-21",{"date":155,"type":21},"2026-10-30",{"name":157,"class":49},"Hospital Samaritano Paulista"]