[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"University of Hamburg-Eppendorf\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":92},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,40,64],{"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":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":29,"lastUpdatePostDateStruct":30,"startDateStruct":33,"completionDateStruct":34,"leadSponsor":36,"locationsCount":39},"100625247","remote-ischemic-preconditioning-and-postoperative-neuronal-injury-100625247",false,"NCT07420153","Remote Ischemic Preconditioning and Postoperative Neuronal Injury","Remote Ischemic Preconditioning and Postoperative Neuronal Injury in Non-Cardiac Surgery Patients: A Randomized Trial","SHIELD","Inclusion criteria:\n\n* patients (≥50 years) scheduled for elective non-cardiac surgery with general anesthesia\n* patients at risk for postoperative delirium, defined as the presence of ≥2 of the following established risk factors: age ≥65 years, American Society of Anesthesiologists physical status classification of ≥III, Charlson Comorbidity, planned surgical duration \\>180 minutes, polypharmacy (regular intake of more than five medications), symptoms of depression (Patient Health Questionnaire-9 ≥10 points)\n\nExclusion criteria:\n\n* patients in whom RIPC cannot be safely applied due to relevant peripheral arterial disease (defined as Fontaine stage ≥II), lymphedema, recent upper-arm surgery, trauma, or skin lesions at the arm\n* patients with acute coronary syndrome (within the past month)\n* patients with surgery in the previous month\n* patients with intracranial surgery\n* patients with pre-existing delirium\n* patients with severe cognitive impairment preventing reliable delirium assessment\n* patients with current treatment with sulfonamides due to potential interference with ischemic preconditioning mechanisms\n* patients with previous participation in the SHIELD trial","ALL","50 Years",{"count":20,"type":21},216,"ESTIMATED","INTERVENTIONAL",[24],"NA","The SHIELD trial is a single-center, randomized, controlled, parallel-group, single-blinded clinical trial investigating whether performing RIPC one day before surgery-compared to not performing RIPC-reduces postoperative neuronal injury, as reflected by the maximum serum NfL concentration within the first 2 postoperative days, in non-cardiac surgery patients at risk for postoperative delirium.",[27],"Postoperative Neuronal Injury","RECRUITING","2026-03-02",{"date":31,"type":32},"2026-03-04","ACTUAL",{"date":29,"type":32},{"date":35,"type":21},"2027-09",{"name":37,"class":38},"University of Hamburg-Eppendorf","OTHER",1,{"id":41,"slug":42,"hasResults":11,"nctId":43,"briefTitle":44,"officialTitle":45,"acronym":46,"eligibilityCriteria":47,"healthyVolunteers":11,"sex":48,"minAge":49,"maxAge":4,"enrollmentInfo":50,"targetDuration":4,"studyType":22,"phases":52,"briefSummary":53,"conditions":54,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":56,"lastUpdatePostDateStruct":57,"startDateStruct":59,"completionDateStruct":61,"leadSponsor":63,"locationsCount":39},"100619789","oscillometric-versus-intraarterial-blood-pressure-monitoring-during-robot-assisted-prostatectomy-100619789","NCT07349186","Oscillometric Versus Intraarterial Blood Pressure Monitoring During Robot-Assisted Prostatectomy","Oscillometric Versus Intraarterial Blood Pressure Monitoring to Reduce Intraoperative Hypotension During Robot-Assisted Prostatectomy: A Non-Inferiority Randomized Trial","PROST-BP","Inclusion Criteria:\n\n* male patient ≥18 years\n* scheduled for elective robot-assisted (Da Vinci) radical prostatectomy in steep Trendelenburg position\n* planned intraarterial blood pressure monitoring\n\nExclusion Criteria:\n\n* patients in whom the attending anesthesiologist considers intraarterial blood pressure monitoring to be mandatory for clinical reasons\n* patients participating in another interventional trial likely to influence intraoperative blood pressure management","MALE","18 Years",{"count":51,"type":21},210,[24],"The PROST-BP trial is a prospective, single-center, randomized, patient-blinded, non-inferiority trial investigating whether intermittent oscillometric blood pressure monitoring is non-inferior to continuous intraarterial blood pressure monitoring in reducing intraoperative hypotension in patients having robot-assisted radical prostatectomy.",[55],"Intraoperative Hypotension","2026-01-30",{"date":58,"type":32},"2026-02-02",{"date":60,"type":32},"2026-01-29",{"date":62,"type":21},"2027-02",{"name":37,"class":38},{"id":65,"slug":66,"hasResults":11,"nctId":67,"briefTitle":68,"officialTitle":69,"acronym":70,"eligibilityCriteria":71,"healthyVolunteers":11,"sex":17,"minAge":49,"maxAge":4,"enrollmentInfo":72,"targetDuration":4,"studyType":22,"phases":74,"briefSummary":76,"conditions":77,"keywords":79,"overallStatus":83,"whyStopped":4,"lastUpdateSubmitDate":84,"lastUpdatePostDateStruct":85,"startDateStruct":87,"completionDateStruct":89,"leadSponsor":91,"locationsCount":4},"100550263","phase-3-model-informed-precision-dosing-for-linezolid-100550263","NCT06444802","Model-informed Precision Dosing for Linezolid","Model-informed Precision Dosing for Linezolid: a Pilot Randomized Clinical Trial","LINEMAP","Inclusion Criteria:\n\n1. ≥ 18 years of age\n2. Linezolid treatment is indicated or has been started due to pneumonia, skin or soft tissue infection; the patient has received no more than 2 infusions of 600 mg linezolid each\n3. with written informed consent of the patient or\n4. with written informed consent of his\u002Fher legal representative or\n5. after using the option of inclusion via spouse according to § 1358 BGB or\n6. after application of the independent consultant procedure\n7. Patients of childbearing age: negative pregnancy test\n\nExclusion Criteria:\n\n1. Patients receiving antibiotics active against Gram-positive bacteria at the same time of linezolid\n2. Infection other than pneumonia, skin or soft tissue infection, especially tuberculosis, endocarditis and osteomyelitis\n3. Death is deemed imminent and inevitable\n4. Pregnancy\n5. Lactation\u002Fbreastfeeding",{"count":73,"type":21},28,[75],"PHASE3","Study Rationale: Previous in vitro and retrospective in vivo studies suggest that optimal linezolid concentrations (between 2 and 7 mg\u002FL) achieve clinical efficacy and microbiological eradication while minimizing side effects like thrombocytopenia and the emergence of resistance. No prospective or randomized clinical trial has confirmed these findings, and there is no consensus on how to adjust linezolid dosing to achieve optimal drug concentrations.\n\nObjectives: The primary objective is to determine if model-informed precision dosing optimizes linezolid dosing to achieve therapeutic trough concentrations compared to a standard dose. Secondary objectives include assessing the PK\u002FPD profile, investigating the prevalence of linezolid resistance among gram-positive bacteria, assessing microbiological resolution of infection, and evaluating the safety and tolerability of linezolid.\n\nMethodology: This study is an open, monocentric pilot randomized controlled trial with two arms: standard dose therapy versus dose adjustment based on model-informed precision dosing using therapeutic drug monitoring and PK\u002FPD targets developed in TMDx software.\n\nSample Size: 28 patients, 14 in each group. Assumptions are based on only 25% of patients in intensive care achieving the optimal therapeutic range with standard dosing, compared to an expected 80% achieving this with model-informed precision dosing.\n\nSelection Criteria: Adult patients (18+ years) already starting linezolid treatment for gram-positive infections, expected to require treatment beyond the next calendar day. Exclusions include imminent death, expected or confirmed pregnancy, expected linezolid treatment of less than 4 days or more than 4 weeks.\n\nOutcomes: The primary endpoint is defined as the difference in the proportion of patients in the intervention and in the control groups who maintained a trough linezolid concentration of 2 to 7 mg\u002FL on Day 7 and Day 13.",[78],"Gram-Positive Bacterial Infections",[80,81,82],"Linezolid","PK-PD Model","TDM","NOT_YET_RECRUITING","2024-05-30",{"date":86,"type":32},"2024-06-06",{"date":88,"type":21},"2024-09-01",{"date":90,"type":21},"2026-06-30",{"name":37,"class":38},""]