[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"early-warning-score\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:early-warning-score":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,43],{"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":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":42},"100401476","rapid-response-teams---how-and-who-100401476",false,"NCT04507737","Rapid Response Teams - How and Who?","Rapid Response Teams - How and Who? A Randomized Controlled Trial Examining the Composition of the RRT in a General Hospital","RRT-Comp","Inclusion Criteria:\n\n* Admitted to any general ward of the hospital AND\n* Aged ≥ 18 years AND\n* In need of RRT attention\n\nExclusion Criteria:\n\n* Age \\\u003C 18\n* Admitted to the delivery ward\n* Admitted to any ward in the anesthetic department\n\n  * ICU\n  * High Dependency Unit\n  * Post Operation Department\n  * Operating Theatre\n  * Same Day Admissions - Surgery Ward\n* Not admitted at the time of call\n\n  * Evaluation track in Emergency department (prior to being seen by a doctor)\n  * Out-Patient departments\n  * X-ray department\n* Any patient who cannot be randomized at the time of call","ALL","18 Years",{"count":20,"type":21},1500,"ESTIMATED","INTERVENTIONAL",[24],"NA","This will be an investigator initiated One-sided blinded Randomized Clinical Trial.\n\nThe study will examine the composition of the Rapid Response Team (RRT). the investigators will examine to see if a Critical Care Outreach Team (CCOT) consisting of an ICU-Nurse and a general ward physician and nurse are non-inferior to a Medical Emergency Team (MET) consisting of an ICU-Doctor and ICU Nurse as well as a general ward physician and nurse. The randomization will be done using an Analogue randomization sequence using sealed opaque envelopes with central randomization.The experimental intervention will be the CCOT. The statistical analyses will be done on the primary outcomes in the intention to treat population and on the secondary outcomes on an per-protocol basis exempting those with protocol violations.",[27,28,29],"Hospital Rapid Response Team","Early Warning Score","Intensive Care Units","RECRUITING","2025-09-11",{"date":33,"type":34},"2025-09-17","ACTUAL",{"date":36,"type":34},"2021-09-01",{"date":38,"type":21},"2026-01-31",{"name":40,"class":41},"Nordsjaellands Hospital","OTHER",1,{"id":44,"slug":45,"hasResults":11,"nctId":46,"briefTitle":47,"officialTitle":48,"acronym":4,"eligibilityCriteria":49,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":50,"targetDuration":4,"studyType":52,"phases":4,"briefSummary":53,"conditions":54,"keywords":4,"overallStatus":55,"whyStopped":4,"lastUpdateSubmitDate":56,"lastUpdatePostDateStruct":57,"startDateStruct":59,"completionDateStruct":61,"leadSponsor":63,"locationsCount":4},"100596895","recovery-room-early-warning-score-100596895","NCT07051421","RECOVERY ROOM EARLY WARNING SCORE","A NEW EARLY WARNING SCORE TO SUPPORT CLINICAL DECISION PROCESSES IN POSTANESTHETIC FOLLOW-UP: RECO-EWS","Inclusion Criteria:\n\n* Those over 18 years of age,\n* Those in ASA I-III class,\n* Those who have undergone planned elective surgery under general anesthesia,\n* Those who have been informed about the study in advance and given their consent.\n\nExclusion Criteria:\n\n* Those under 18 years of age,\n* Those who underwent emergency intervention,\n* Those in the ASA-Ⅳ class,\n* Those who underwent regional anesthesia,\n* Those with a history of cognitive retardation, visual-hearing impairment or psychiatric disease that prevents communication, those who have previously been diagnosed with neurocognitive disorders,\n* Patients who could not complete the procedure, patients with data loss,\n* Patients whose general anesthesia duration is less than 90 minutes will not be included in the study.",{"count":51,"type":21},208,"OBSERVATIONAL","In this study, we aimed to develop a scoring system that facilitates patient risk stratification in the recovery room during the postanesthetic follow-up period and can objectively identify patients in need of early intervention.",[28],"NOT_YET_RECRUITING","2025-06-26",{"date":58,"type":34},"2025-07-04",{"date":60,"type":21},"2025-07-01",{"date":62,"type":21},"2025-12-01",{"name":64,"class":41},"Istinye University"]