[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"polyps\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:polyps":24},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,46],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":22,"conditions":23,"keywords":29,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":45},"100444184","early-diagnosis-real-time-healthcare-system-for-cancer-trial-100444184",false,"NCT05064124","Early DiAgnosis Real-Time Healthcare System for CANcer Trial","EARTHSCAN","Inclusion Criteria:\n\n* Participants scheduled to undergo a screening, surveillance or symptomatic colonoscopy with an endoscopist participating in the study phase of the trial.\n* Male and female participants aged 18 years or older at the time of informed consent.\n* Participants able to comprehend, sign and date the written informed consent document to participate in the study.\n\nExclusion Criteria:\n\n* Emergency and\u002For inpatient colonoscopies\n* Participants with inflammatory bowel disease (IBD)\n* Participants with current Colorectal Cancer (CRC)\n* Participants with a contraindication for biopsy or polypectomy. These include:\n\n  * Participants who have not withheld medications pre-disposing to bleeding at time of colonoscopy as per local site \u002Fnational guidelines.\n  * Participants with a history of haemostasis disorders (haemostasis disorders will include but will not be limited to: participants with haemophilia or other congenitally acquired clotting factor deficiencies, participants with cirrhosis with coagulopathy, participants known to have thrombocytopenia (\\\u003C80,000 platelet\u002Ful) and individuals with Von Willebrand's disease or other known platelet malfunction disorders)\n* Participant is enrolled in another research study with an investigational medicinal product (IMP) or non-IMP that pre-disposes them to bleeding","ALL","18 Years",{"count":19,"type":20},420,"ESTIMATED","OBSERVATIONAL","The purpose of the study is to assess whether the AI characterisation system of the CADDIE device improves the endoscopists accuracy in the optical diagnosis of diminutive colorectal polyps in the bowel during colonoscopy. Participants will either have a colonoscopy with the assistance of the CADDIE device characterisation AI system (\"intervention group\") or have a colonoscopy in line with routine clinical practice i.e., without the CADDIE device characterisation AI system (\"control group\"). The randomisation method of this trial will allocate enrolled participants to the \"intervention\" group and to the \"control\" group by a technique similar to flipping a coin.",[24,25,26,27,28],"Polyps","Adenoma Colon","Colorectal Polyp","Colon Polyp","Polyps of Colon",[30,31,32],"Artificial intelligence","Endoscopy","ADR","RECRUITING","2024-12-10",{"date":36,"type":37},"2024-12-16","ACTUAL",{"date":39,"type":37},"2024-07-18",{"date":41,"type":20},"2025-05",{"name":43,"class":44},"University College, London","OTHER",1,{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":52,"eligibilityCriteria":53,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":54,"targetDuration":56,"studyType":21,"phases":4,"briefSummary":57,"conditions":58,"keywords":65,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":75,"completionDateStruct":77,"leadSponsor":79,"locationsCount":4},"100553047","algerian-cholecystectomy-outcomes-and-determinants-study-al-cods-100553047","NCT06481007","ALgerian Cholecystectomy Outcomes and Determinants Study (AL-CODS)","Algerian Cholecystectomy Outcomes and Determinants Study","AL-CODS","Inclusion Criteria:\n\n* Patients aged 18 years and older.\n* Undergoing cholecystectomy.\n* Surgery performed in public or private hospitals in Algeria.\n* Surgery performed from January 1, 2025, to June 30, 2025.\n\nExclusion Criteria:\n\n* Patients younger than 18 years.\n* Patients refusing to participate.\n* Cholecystectomy performed for Gallbladder cancer.\n* Cholecystectomy performed outside the inclusion period.\n* Cholecystectomies performed in conjunction with other major surgeries.",{"count":55,"type":20},500,"1 Month","Cholecystectomy, the surgical removal of the gallbladder, is a common procedure performed to treat benign gallbladder diseases such as cholelithiasis (gallstones), cholecystitis (inflammation of the gallbladder), and biliary dyskinesia. While generally considered safe, this surgery can be associated with significant morbidity and mortality, particularly in certain populations or healthcare settings. Understanding these outcomes and the factors influencing them is crucial for improving patient care and surgical practices.\n\nIn Algeria, the healthcare landscape presents unique challenges and opportunities for evaluating surgical outcomes. Limited studies have specifically focused on the morbidity and mortality associated with cholecystectomy in this context. This study aims to fill that gap by providing comprehensive data on 30-day postoperative outcomes following cholecystectomy for benign gallbladder diseases in Algeria. Such data is essential for benchmarking current practices, identifying areas for improvement, and ultimately enhancing patient safety and surgical efficacy.",[59,60,61,24,62,63,64],"Cholecystectomy","Adults","Gall Stone","Pancreatitis Biliary","Gallbladder Dyskinesia","Cholecystitis",[66,59,67,68,69,70],"Algeria","mortality","morbidity","30 days","determinants","NOT_YET_RECRUITING","2024-06-26",{"date":74,"type":37},"2024-07-01",{"date":76,"type":20},"2025-01-01",{"date":78,"type":20},"2025-07-02",{"name":80,"class":44},"University of Oran 1"]