[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"anesthesiology\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:anesthesiology":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,49,84],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":31,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":48},"100560360","ultrasound-guided-transversus-abdominis-plan-tap-block-in-endovascular-cardiac-interventions-100560360",false,"NCT06576128","Ultrasound-Guided Transversus Abdominis Plan (TAP) Block in Endovascular Cardiac Interventions","Analgesic Effect of Ultrasound-Guided Transversus Abdominis Plan (TAP) Block in Femoral Endovascular Cardiac Interventions: A Prospective-randomized Study","Inclusion Criteria:\n\n* The patient is over 18 years of age\n* Coronary angiography, cardiac catheterization and percutaneous coronary intervention will be applied to the patient,\n* The above-mentioned procedures will be taken under elective conditions,\n* Providing an optimal image when imaging the patient with ultrasound,\n* INR\\\u003C 1.5\n* If the patient gives consent, S\u002Fhe will be included in the study.\n\nExclusion Criteria:\n\n* Patients under 18 years of age,\n* Patients treated under emergency conditions,\n* morbid obesity (BMI\\>35 kg\u002Fm2),\n* pregnant women,\n* New York Heart Association (NYHA) stage 4 patients with advanced decompensated heart failure,\n* Patients with symptoms such as redness, temperature increase, infection, hematoma in the application area before the procedure,\n* Patients with a history of allergy to local anesthetics,\n* Patients who cannot be communicated,\n* Those with severe psychosis or progressive neurological deficits and muscle disease,\n* Patients who do not consent to the application will be excluded from the study.","ALL","18 Years",{"count":19,"type":20},100,"ESTIMATED","INTERVENTIONAL",[23],"NA","Sensory innervation of the femoral region which is the entry point for endovascular cardiac interventions such as coronary angiography,cardiac catheterization and percutaneous coronary intervention is complex.It is thought that the ilioinguinal and iliohypogastric nerves contribute mostly.With transversus abdominis plane block(TAPB),it is planned to provide analgesia by creating a block in these nerve branches that contribute to the sensory innervation of the intervention area.In addition;it was aimed to investigate patient's and physician's satisfaction during the procedure.",[26,27,28,29,30],"Anesthesiology","Percutaneous Coronary Intervention","Cardiac Catheterization","Analgesia","Satisfaction, Patient",[32,33,34,27,28,35],"ultrasonography","anesthesiology","transversus abdominis plane block","analgesia","RECRUITING","2026-05-04",{"date":39,"type":40},"2026-05-08","ACTUAL",{"date":42,"type":40},"2024-09-10",{"date":44,"type":20},"2026-12-15",{"name":46,"class":47},"Istanbul University - Cerrahpasa","OTHER",1,{"id":50,"slug":51,"hasResults":11,"nctId":52,"briefTitle":53,"officialTitle":54,"acronym":55,"eligibilityCriteria":56,"healthyVolunteers":11,"sex":16,"minAge":57,"maxAge":4,"enrollmentInfo":58,"targetDuration":4,"studyType":21,"phases":60,"briefSummary":61,"conditions":62,"keywords":67,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":75,"lastUpdatePostDateStruct":76,"startDateStruct":78,"completionDateStruct":80,"leadSponsor":82,"locationsCount":48},"100622551","continuous-vital-sign-monitoring-versus-routine-spot-checks-in-patients-after-non-cardiac-surgery-100622551","NCT07385092","Continuous Vital Sign Monitoring Versus Routine Spot-checks in Patients After Non-cardiac Surgery","The Effect of Continuous Monitoring Versus Routine Spot-checks on Altered Vital Signs in Patients Recovering From Non-cardiac Surgery on Normal Wards: the \"COME ON, NOW!\" Trial","COME ON NOW","Inclusion Criteria:\n\nConsenting patients ≥45 years scheduled for elective non-cardiac (abdominal and thoracic) surgery with planned postoperative admission to a normal ward after an overnight stay in an advanced post-anesthesia care unit.\n\nExclusion Criteria:\n\n* Emergency surgery\n* Pregnancy\n* Impossibility to perform continuous monitoring with the Radius VSM sensor (Masimo, Irvine, CA)\n* Atrial fibrillation\n* Patients designated Do Not Resuscitate, or are receiving end-of-life care","45 Years",{"count":59,"type":20},264,[23],"The \"COME ON, NOW!\" trial is a randomized, single-center trial in patients recovering from non-cardiac surgery on normal wards investigating whether continuous vital sign monitoring - compared to routine spot-checks by nurses - reduces the total duration of abnormal vital signs per hour during the first 48 hours after admission to the normal ward.",[63,64,65,66,26],"Vital Sign Monitoring","Post Operative Complications","Non-cardiac Surgery","RCT",[68,69,70,71,33,72,73,74],"continuous vital signs","vital signs","vital sign monitoring","post-operative care","anesthesia","hypotension","post-operative complications","2026-02-27",{"date":77,"type":40},"2026-03-02",{"date":79,"type":40},"2026-02-24",{"date":81,"type":20},"2026-12-31",{"name":83,"class":47},"Universitätsklinikum Hamburg-Eppendorf",{"id":85,"slug":86,"hasResults":11,"nctId":87,"briefTitle":88,"officialTitle":89,"acronym":90,"eligibilityCriteria":91,"healthyVolunteers":92,"sex":16,"minAge":4,"maxAge":4,"enrollmentInfo":93,"targetDuration":4,"studyType":21,"phases":95,"briefSummary":96,"conditions":97,"keywords":4,"overallStatus":103,"whyStopped":4,"lastUpdateSubmitDate":104,"lastUpdatePostDateStruct":105,"startDateStruct":107,"completionDateStruct":109,"leadSponsor":111,"locationsCount":48},"100622612","ultrasound-guided-non-invasive-simulation-in-anesthesia-residency-training-100622612","NCT07385885","Ultrasound-guided Non-invasive Simulation in Anesthesia Residency Training","Application of Ultrasound-guided Non-invasive Simulated Puncture Technique in Standardized Residency Training in Anesthesiology","non-invasive","Inclusion Criteria:\n\n\\~Anesthesiology residents participating in the standardized residency training program in the Department of Anesthesiology at Nanjing First Hospital between October 2024 and October 2026.\n\nExclusion Criteria:\n\n* Residents with prior experience in performing nerve block procedures.\n* Residents currently participating in other teaching or research studies related to nerve blocks.",true,{"count":94,"type":20},30,[23],"Study Aim: This trial evaluates if a novel non-invasive, AI-assisted simulation training improves ultrasound-guided needle visualization skills in anesthesia residents.\n\nDesign: Trainees were randomized into two groups:\n\nIntervention: AI-based, non-invasive simulated needle puncture training. Control: Conventional ultrasound teaching. Key Outcomes: The primary outcome is objective needle tip visibility. Secondary outcomes include anatomical identification, correct view acquisition, operator confidence, and overall scanning performance.\n\nAssessment: Outcomes are measured via blinded expert evaluation and theoretical tests.\n\nThe goal of this randomized controlled clinical trial is to determine whether an ultrasound-guided non-invasive simulated needle puncture training technique can improve ultrasound-guided needle visualization skills in anesthesiology residents undergoing standardized residency training. The study is conducted in anesthesiology residents enrolled in a standardized residency training program.\n\nThe main questions it aims to answer are:\n\n1. Does non-invasive simulated needle puncture training improve objective needle tip visibility during ultrasound-guided peripheral nerve block procedures?\n2. Does this training method improve anatomical structure identification, acquisition of correct block views, operator confidence, and overall scanning performance compared with conventional ultrasound teaching? Researchers will compare a non-invasive simulated needle puncture training group with a conventional ultrasound teaching group to see if the simulated training technique leads to superior needle visualization and procedural performance.\n\nParticipants will:\n\nReceive standardized theoretical instruction on ultrasound- guided peripheral nerve blocks; Be randomly assigned to either non-invasive simulated needle puncture training using an artificial intelligence-assisted system or conventional ultrasound scanning training; Perform ultrasound scanning and simulated or conventional practice on healthy volunteers; Undergo theoretical examinations and blinded expert assessments of ultrasound scanning performance and needle visualization outcomes.",[98,99,100,26,101,102],"Ultrasound","Needle","Residency","Training","Non-invasive","NOT_YET_RECRUITING","2026-02-03",{"date":106,"type":40},"2026-02-04",{"date":108,"type":20},"2026-02-01",{"date":110,"type":20},"2028-12-30",{"name":112,"class":47},"Nanjing First Hospital, Nanjing Medical University"]