[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"systemic-inflammatory-response-syndrome-sirs\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:systemic-inflammatory-response-syndrome-sirs":40},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":4,"hasResults":10,"nctId":11,"briefTitle":12,"officialTitle":12,"acronym":4,"eligibilityCriteria":13,"healthyVolunteers":10,"sex":14,"minAge":15,"maxAge":4,"enrollmentInfo":16,"targetDuration":4,"studyType":19,"phases":20,"briefSummary":22,"conditions":23,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":29,"lastUpdatePostDateStruct":30,"startDateStruct":33,"completionDateStruct":35,"leadSponsor":37,"locationsCount":4},"100628314",false,"NCT07460024","Implementation of Timely Management of Sepsis and Septic Shock Protocol in the Emergency Department and Intensive Care Unit: A Quality Improvement Project at AFHJ","Inclusion Criteria:\n\n* Adult patients aged 18 years or older.\n* Clinical suspicion of sepsis or a confirmed diagnosis of sepsis upon admission to the Emergency Department (ED) or Intensive Care Unit (ICU).\n* Presence of symptoms meeting the criteria for the sepsis management protocol during the study period.\n\nExclusion Criteria:\n\n* Patients transferred from other healthcare facilities after sepsis treatment had already been initiated.\n* End-of-life cases or patients with \"Do Not Attempt Resuscitation\" (DNAR) status where data sets are incomplete.\n* Cases with insufficient medical documentation that prevents accurate outcome measurement or bundle compliance tracking.","ALL","18 Years",{"count":17,"type":18},120,"ESTIMATED","INTERVENTIONAL",[21],"NA","Study Title: Implementation of a Sepsis Management Protocol at Armed Forces Hospital Jazan (AFHJ).\n\nPurpose: The purpose of this quality improvement project is to determine if implementing a standardized, evidence-based \"sepsis bundle\" can improve the care and survival of patients with sepsis and septic shock in the Emergency Department (ED) and Intensive Care Unit (ICU).\n\nWhat the Study Involves:\n\nResearchers will implement a specific set of clinical guidelines based on the international Surviving Sepsis Campaign. This include:\n\nUsing a scoring system (NEWS2 and SOFA) to identify sick patients earlier.\n\nEnsuring patients receive five critical treatments (the \"one-hour bundle\") within 60 minutes of diagnosis, including blood tests, IV fluids, and antibiotics.\n\nComparison:\n\nThe study will compare the outcomes of 74 patients treated before the protocol was introduced (the \"Pre-protocol group\") to 46 patients treated after the new protocol was put into effect (the \"Protocol group\").\n\nExpected Outcome:\n\nThe goal is to increase the number of patients who receive all necessary treatments within one hour from less than 15% to at least 60%. The study also aims to see if this protocol leads to shorter hospital stays and lower mortality rates.",[24,25,26,27],"Sepsis","Septic Shock","Systemic Inflammatory Response Syndrome (SIRS)","Critical Illness","NOT_YET_RECRUITING","2026-03-09",{"date":31,"type":32},"2026-03-10","ACTUAL",{"date":34,"type":18},"2026-03",{"date":36,"type":18},"2026-11",{"name":38,"class":39},"Al-Azhar University","OTHER",""]