[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100389770":3},{"organization":4,"armGroups":7,"interventions":10,"overallOfficials":18,"centralContacts":22,"locations":27,"responsibleParty":76,"collaborators":79,"id":82,"slug":83,"hasResults":84,"nctId":85,"briefTitle":86,"officialTitle":87,"acronym":10,"eligibilityCriteria":88,"healthyVolunteers":84,"sex":89,"minAge":90,"maxAge":10,"enrollmentInfo":91,"targetDuration":10,"studyType":94,"phases":10,"briefSummary":95,"conditions":96,"keywords":10,"overallStatus":30,"whyStopped":10,"lastUpdateSubmitDate":98,"lastUpdatePostDateStruct":99,"startDateStruct":102,"completionDateStruct":104,"leadSponsor":106,"locationsCount":107},{"fullName":5,"class":6},"Charite University, Berlin, Germany","OTHER",[8,12,15],{"label":9,"type":10,"description":11,"interventionNames":10},"Cohort before training",null,"500 patients should be asked to participate in the project in the phase of zero value measurement. The documentation of the routine data before the training phase relates to patients aged ≥70 years, male and female, who are undergoing surgery.",{"label":13,"type":10,"description":14,"interventionNames":10},"Cohort after training 1","From October 1st, 2020, the documentation of the routine data will begin after the training phase: 2,500 patients in 12 months, each aged ≥70 years, male and female, who will have surgery until the end of the contract on June 30th, 2023.",{"label":16,"type":10,"description":17,"interventionNames":10},"Cohort after documentation of routine data until June 2023","From July 1st, 2023, the documentation of the routine data will go on: 1,700 patients in 12 months, each aged ≥70 years, male and female, who will have surgery until the end of the contract on June 30th, 2028.",[19],{"name":20,"affiliation":5,"role":21},"Claudia Spies, MD, Prof.","STUDY_DIRECTOR",[23],{"name":20,"role":24,"phone":25,"phoneExt":10,"email":26},"CONTACT","+49 30 450 55 11 02","claudia.spies@charite.de",[28,54],{"facility":29,"status":30,"city":31,"state":10,"zip":32,"country":33,"countryCode":34,"cosmosGeoPoint":35,"geoPoint":40,"contacts":41},"Department of Anesthesiology and Intensive Care Medicine (CBF), Charité - Universitätsmedizin Berlin","RECRUITING","Berlin","12203","Germany","DE",{"type":36,"coordinates":37},"Point",[38,39],13.41053,52.52437,{"lat":39,"lon":38},[42,46,49,52],{"name":43,"role":24,"phone":44,"phoneExt":10,"email":45},"Sascha Treskatsch, MD. Prof.","+49 30 450 55 15 22","sascha.treskatsch@charite.de",{"name":47,"role":48,"phone":10,"phoneExt":10,"email":10},"Sascha Treskatsch, MD, Prof.","PRINCIPAL_INVESTIGATOR",{"name":50,"role":51,"phone":10,"phoneExt":10,"email":10},"Lennart Junge, MD","SUB_INVESTIGATOR",{"name":53,"role":51,"phone":10,"phoneExt":10,"email":10},"Golschan Asgarpur, MD",{"facility":55,"status":30,"city":31,"state":10,"zip":56,"country":33,"countryCode":34,"cosmosGeoPoint":57,"geoPoint":59,"contacts":60},"Department of Anesthesiology and Intensive Care Medicine (CCM\u002FCVK) Berlin, Carité - Universitätsmedizin Berlin","13353",{"type":36,"coordinates":58},[38,39],{"lat":39,"lon":38},[61,63,64,66,68,70,72,74],{"name":62,"role":24,"phone":25,"phoneExt":10,"email":26},"Caudia Spies, MD, Pof.",{"name":20,"role":48,"phone":10,"phoneExt":10,"email":10},{"name":65,"role":51,"phone":10,"phoneExt":10,"email":10},"Fatima Halzl-Yürek, MD",{"name":67,"role":51,"phone":10,"phoneExt":10,"email":10},"Daniel Hadzidiakos, MD",{"name":69,"role":51,"phone":10,"phoneExt":10,"email":10},"Laerson Hoff",{"name":71,"role":51,"phone":10,"phoneExt":10,"email":10},"Maurice Breithaupt, MD",{"name":73,"role":51,"phone":10,"phoneExt":10,"email":10},"Antje Kirchstein, MD",{"name":75,"role":51,"phone":10,"phoneExt":10,"email":10},"Friedrich Borchers, MD",{"type":48,"investigatorFullName":77,"investigatorTitle":78,"investigatorAffiliation":5,"oldNameTitle":10,"oldOrganization":10},"Claudia Spies","Head of the Department of Anesthesiology and Operative Intensive Care Medicine (CCM\u002FCVK\u002FCBF)",[80],{"name":81,"class":6},"BARMER","100389770","quality-contract-prevention-of-postoperative-delirium-in-the-care-of-older-patients-qv-pod-2-100389770",false,"NCT04355195","Quality Contract: Prevention of Postoperative Delirium in the Care of Older Patients (QV-POD-2)","Quality Contract Prevention of Postoperative Delirium in the Care of Older Patients (QV-POD-2)","Inclusion criteria:\n\n* Age ≥ 70 years\n* male and female patients\n* Patients who are insured with BARMER, HEK, KKH, DAK, TK or hkk Health insurances\n* Patients eligible for inclusion: by the patient, preoperatively\n* Incapacitated patients for inclusion: Written informed consent by a legal representative\n* surgery (elective and not elective)\n\nExclusion criteria:\n\n* Moribund patients\n* Not enough language skills","ALL","70 Years",{"count":92,"type":93},18100,"ESTIMATED","OBSERVATIONAL","The project \"QV-POD-2\" is a prolongation based on \"QV-POD-1\", which was a quality contract program of the IQTIG - Institute for Quality and Transparency in Health Care. The aim is to improve inpatient care for older patients who are undergoing inpatient surgery and thus to specifically reduce the postoperative risk of delirium. This is achieved through the implementation of evidence-based and consensus-based measures to prevent postoperative delirium in a comprehensive structured concept in routine care. The transparent documentation in an electronic patient file enables the relationships between the symptoms to be depicted in accordance with the clinical circumstances and the genesis of the postoperative delirium to be recorded and treated at an early stage. The content of the additional elements from the routine data (see primary and secondary outcome measures) in QV-POD-2 is analysed internally.\n\nSubproject Retro-Pressure started in August 2022:\n\nRetrospective, exploratory cohort study using electronic anesthesia and hospital records from Jan 1, 2016 to Jan 1, 2020, including patients ≥70 years undergoing surgery with anesthesia. The objective is to quantify associations between intraoperative blood pressure dynamics-variability, rate of change, relative hypo-\u002Fhypertension versus baseline, and time-integrated BP (area under\u002Fabove reference)-and postoperative organ dysfunction Primary endpoints: Emergence delirium incidence (PACU\u002FITS) based on Nu-DESC scores and CAM-ICU scores; incidence of postoperative acute renal failure (creatinine and urea levels, as well as urine output); intraoperative blood pressure variation\\*; intraoperative blood pressure variation rate\\*; intraoperative blood pressure integral\\* Secondary endpoints: Blood count (hemoglobin and hematocrit values); intraoperative transfusions of blood reserves Addendum from the ethics amendment vote of 25\u002F07\u002F2022\n\nSubproject Delta-Scan started in August 2022:\n\nEvaluation of brain function using \"Delta Scan\" Primary objective: Evaluation of the prognostic significance of Delta Scan measurements in relation to postoperative delirium Secondary objectives: Examination of the delirium-related predictive relevance of individual influencing factors (directly but also indirectly through Delta Scan values) and examination of the effect of Delta Scan measurements on standard delirium screening methods. Study and control group's Inclusion criteria: Age \\>= 70 years and major surgery with anesthesia; additional exclusion criterion in the control group: Inclusion in the QV-POD-1 project (receipt of postoperative preventive measures) Addendum from the ethics amendment vote of 25\u002F07\u002F2022\n\nSubproject started in June,18th, 2026:\n\nFor selected patients who are scheduled to undergo a procedure in June, July or August 2026 as part of the QV-POD-2 study, a wristband called CardioWatch 287-2 (manufacturer: Corsano Health B.V., Wilhelmina van Pruisenweg 35, 2595 AN The Hague, The Netherlands, loaned by Medtronic, will be etsablished. For same-day surgery patients, monitoring begins before the operation and continues until discharge from the hospital. For pre-hospitalized patients, measurements can begin at least one day before surgery upon request. The recorded values include blood pressure, heart rate, heart rate variability, respiratory rate, oxygen saturation, body temperature, physical activity, and an electrocardiogram once a day.",[97],"Delirium in Old Age","2026-06-22",{"date":100,"type":101},"2026-06-26","ACTUAL",{"date":103,"type":101},"2020-04-20",{"date":105,"type":93},"2029-06",{"name":5,"class":6},2]