[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"general-anaesthesia\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:general-anaesthesia":25},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,40,71,107],{"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":4,"studyType":22,"phases":4,"briefSummary":23,"conditions":24,"keywords":4,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":28,"lastUpdatePostDateStruct":29,"startDateStruct":32,"completionDateStruct":34,"leadSponsor":36,"locationsCount":39},"100554343","impact-of-estimated-concentration-of-propofol-on-implicit-memory-formation-100554343",false,"NCT06497855","Impact of Estimated Concentration of Propofol on Implicit Memory Formation","Impact of Target Controlled Infusion Estimated Concentration of Propofol on Implicit Memory Formation During Propofol-Remifentanil General Anaesthesia","Inclusion Criteria:\n\n* General anaesthesia with TIVA-TCI\n\nExclusion Criteria:\n\n* ASA \\> III\n* Benzodiazepines premedication\n* Neurological\u002FPsychiatric disease","FEMALE","18 Years","90 Years",{"count":20,"type":21},80,"ESTIMATED","OBSERVATIONAL","Implicit memory formation and learning during general anaesthesia is a still debated question and no anesthetic regimen (ie intravenous anaesthesia vs inhalatory one) nor analgesic regimen (i.e. low or high opioids usage) has been identified for prevention.\n\nWith this study the investigators aim to investigate if, during Total Intravenous Anaesthesia with Target Controlled Infusion (TIVA-TCI) different concentrations of Propofol at loss of responsiveness, maintenance and return of responsiveness can have a role in implicit memory formation.",[25,26],"General Anaesthesia","Implicit Memory","RECRUITING","2026-06-05",{"date":30,"type":31},"2026-06-08","ACTUAL",{"date":33,"type":31},"2024-07-01",{"date":35,"type":21},"2026-11-15",{"name":37,"class":38},"University of Padova","OTHER",1,{"id":41,"slug":42,"hasResults":11,"nctId":43,"briefTitle":44,"officialTitle":44,"acronym":4,"eligibilityCriteria":45,"healthyVolunteers":46,"sex":47,"minAge":17,"maxAge":4,"enrollmentInfo":48,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":50,"conditions":51,"keywords":55,"overallStatus":60,"whyStopped":4,"lastUpdateSubmitDate":61,"lastUpdatePostDateStruct":62,"startDateStruct":64,"completionDateStruct":66,"leadSponsor":68,"locationsCount":4},"100632182","intercultural-adaptation-and-validation-of-the-ukrainian-quality-of-recovery-15-questionnaire-100632182","NCT07510360","Intercultural Adaptation and Validation of the Ukrainian Quality of Recovery-15 Questionnaire","Inclusion criteria\n\n1. Age 18 or older\n2. Patient scheduled for elective or emergency surgery under general or regional anaesthesia\n3. Able to read and understand Ukrainian\n\nExclusion criteria\n\n1. Patient unable or unwilling to provide informed consent\n2. Any severe preexisting medical condition or cognitive impairment that limits objective assessment after operation\n3. Known substance use disorder associated with cognitive impairment\n\nWithdrawal criteria\n\n1\\. Presence of life-threatening post-operative complications",true,"ALL",{"count":49,"type":21},200,"The Quality of Recovery 15-questionnaire (QoR-15) is used to assess postoperative quality of recovery after surgery and anesthesia from the patient's perspective. It evaluates five dimensions including pain, physical comfort, physical independence, psychological support, and emotional state. The aim of this study is to validate a Ukrainian version of the QoR-15 scale (QoR-15Ukr) to measure postoperative recovery in Ukrainian-speaking patients.",[52,25,53,54],"Postoperative Recovery","Validation","Questionnaire",[56,57,58,59],"postoperative recovery","validation","Ukrainian","QoR-15","NOT_YET_RECRUITING","2026-03-30",{"date":63,"type":31},"2026-04-03",{"date":65,"type":21},"2026-05-01",{"date":67,"type":21},"2026-11-30",{"name":69,"class":70},"Rostyslav Voloshchuk","OTHER_GOV",{"id":72,"slug":73,"hasResults":11,"nctId":74,"briefTitle":75,"officialTitle":76,"acronym":4,"eligibilityCriteria":77,"healthyVolunteers":11,"sex":47,"minAge":78,"maxAge":79,"enrollmentInfo":80,"targetDuration":4,"studyType":82,"phases":83,"briefSummary":85,"conditions":86,"keywords":92,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":98,"lastUpdatePostDateStruct":99,"startDateStruct":101,"completionDateStruct":103,"leadSponsor":105,"locationsCount":39},"100523211","effect-of-fpca-on-incidence-of-emergency-delirium-in-children-after-surgery-100523211","NCT06092671","Effect of FPCA on Incidence of Emergency Delirium in Children After Surgery","Effect of Family-centred Perioperative Care for Anaesthesia on Incidence of Emergency Delirium in Children After Surgery: a Protocol for a Randomised Controlled Trial","Inclusion criteria:\n\n1. Children aged 2-6 years undergoing elective surgery with an estimated surgical duration of no longer than 2 hours;\n2. Receiving first general anaesthesia by inhalation, and American Society of Anaesthesiology (ASA) physical status I to II;\n3. A parent signed the informed consent form.\n\nExclusion criteria:\n\n1. Suffering important organ diseases;\n2. History of developmental retardation, neuropsychiatric diseases, psychological or cognitive impairment;\n3. History of severe hearing or visual impairment;\n4. Children are not suitable for inhalation anaesthesia considered by the researchers;\n5. The parent involving in this trial spends less than three months a year with the child;\n6. The parent is not competent for companionship considered by the researchers;\n7. Neither father nor mother is able to participate in the screening interview and the trial.","2 Years","6 Years",{"count":81,"type":21},444,"INTERVENTIONAL",[84],"NA","Emergence delirium (ED) stands out as a prevalent postoperative complication among paediatric patients, correlating with extended hospitalization periods, escalated healthcare expenses, and increased incidence of postoperative maladaptive behaviours (POMBs). There is a lack of well-established pharmacological or non-pharmacological interventions demonstrating efficacy in reducing the occurrence of ED. Therefore, our objective is to assess the potential of family-centred perioperative care for anaesthesia (FPCA) in mitigating the incidence of ED in children, compared with routine anaesthesia.",[87,88,89,90,25,91],"Postoperative Complications","Child","Family","Emergence Delirium","Perioperative Care",[93,94,95,96,97],"perioperative care","emergency delirium","paediatric","general anaesthesia","postoperative maladaptive behaviours","2025-12-21",{"date":100,"type":31},"2025-12-29",{"date":102,"type":31},"2023-10-24",{"date":104,"type":21},"2026-12",{"name":106,"class":38},"Second Affiliated Hospital of Wenzhou Medical University",{"id":108,"slug":109,"hasResults":11,"nctId":110,"briefTitle":111,"officialTitle":111,"acronym":112,"eligibilityCriteria":113,"healthyVolunteers":11,"sex":47,"minAge":114,"maxAge":4,"enrollmentInfo":115,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":117,"conditions":118,"keywords":121,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":127,"lastUpdatePostDateStruct":128,"startDateStruct":130,"completionDateStruct":132,"leadSponsor":133,"locationsCount":39},"100616743","regional-versus-general-anesthesia-for-hip-fracture-and-postoperative-oxygenation-100616743","NCT07309575","Regional Versus General Anesthesia for Hip Fracture and Postoperative Oxygenation","REGENERATION","Inclusion Criteria:\n\n* hospital admission for hip fracture;\n* scheduled for hip fracture surgery;\n* age above 65 years, both genders;\n* capable of consent or consent by responsible person;\n\nExclusion Criteria:\n\n* hip fracture during hospitalization (not present upon admission)\n* patient refusal to participate","65 Years",{"count":116,"type":21},102,"With this study, the investigators intend to measure oxygen saturation before and after hip surgery in the context of proximal femur fracture, comparing two types of anesthesia (general or spinal). The investigators also intend to study the effects of the two anesthetic techniques on sleep apnea, delirium, respiratory complications, and length of hospital stay.\n\nThis is an observational study, in which oxygen is measured at the fingertip with a sensor and a bracelet, without any intervention, inconvenience, or discomfort for the participant. Data will be collected on: respiratory complications, sleep apnea, delirium, length of hospital stay, and survival.\n\nData will be collected in the operating room and wards of Santa Maria Hospital, Lisbon, Portugal over a period of approximately 24 hours after the participant's operation. Information about participant's health and co-morbidities will be recorded.\n\nThere will be no implication for the participants' clinical care, since the study measurements will not be sent to the health professionals in charge. The operation, recovery, and treatments will not be influenced at any time by participation in the study.",[119,25,120],"Hip-fracture","Regional Anaesthesia",[122,123,124,125,126],"anaesthesia","hip femur fracture","postoperative pulmonary complications","oxygenation","sleep apnea","2025-12-19",{"date":129,"type":31},"2025-12-30",{"date":131,"type":31},"2025-11-27",{"date":104,"type":21},{"name":134,"class":38},"University of Lisbon"]