[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"endoscopy\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:endoscopy":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,11,0,[8,47,79,110,131,155,181,205,234,257,280],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":31,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":4},"100643045","opioid-free-versus-opioid-based-sedation-for-endoscopic-procedures-100643045",false,"NCT07649746","Opioid-Free Versus Opioid-Based Sedation for Endoscopic Procedures","Evaluation of an Opioid-Free Approach in Sedation Method Selection in Endoscopy Units: A Prospective Randomized Observational Double-Blind Comparison of Dexmedetomidine (Opioid-Free) and Remifentanil-Dexmedetomidine (Opioid-Based) Combination","Inclusion Criteria:\n\n* Age 18 to 85 years\n* ASA physical status I-III\n* Scheduled for ERCP, gastroscopy, or colonoscopy\n\nExclusion Criteria:\n\n* Refusal to participate in the study\n* Inability to communicate\n* Alcohol or substance abuse\n* Neuropsychiatric disease\n* Severe respiratory failure\n* Severe heart failure\n* Pregnancy\n* Body mass index (BMI) \\>30 kg\u002Fm²\n* Hearing impairment\n* History of allergy to study medications\n* Requirement for orotracheal intubation or general anesthesia\n* Procedures lasting less than 20 minutes","ALL","18 Years","85 Years",{"count":20,"type":21},80,"ESTIMATED","INTERVENTIONAL",[24],"NA","This study will compare two different sedation approaches used during gastroscopy, colonoscopy, and endoscopic retrograde cholangiopancreatography (ERCP). One group will receive dexmedetomidine alone (opioid-free sedation), while the other group will receive dexmedetomidine combined with remifentanil (opioid-based sedation).\n\nThe purpose of the study is to determine whether an opioid-free sedation approach can reduce opioid-related adverse symptoms, such as nausea, vomiting, dizziness, drowsiness, dry mouth, headache, and fatigue. The study will also evaluate quality of recovery, patient and healthcare staff satisfaction, hemodynamic effects, complications, and time to discharge after the procedure.",[27,28,29,30],"Sedation","Endoscopy","Colonoscopy","Endoscopic Retrograde Cholangiopancreatography (ERCP)",[32,33,34,27,28],"Dexmedetomidine","Opioid-Free Sedation","Remifentanil","NOT_YET_RECRUITING","2026-06-10",{"date":38,"type":39},"2026-06-16","ACTUAL",{"date":41,"type":21},"2026-06",{"date":43,"type":21},"2028-02",{"name":45,"class":46},"Bakirkoy Dr. Sadi Konuk Research and Training Hospital","OTHER_GOV",{"id":48,"slug":49,"hasResults":11,"nctId":50,"briefTitle":51,"officialTitle":51,"acronym":4,"eligibilityCriteria":52,"healthyVolunteers":53,"sex":16,"minAge":4,"maxAge":4,"enrollmentInfo":54,"targetDuration":4,"studyType":22,"phases":56,"briefSummary":57,"conditions":58,"keywords":62,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":68,"lastUpdatePostDateStruct":69,"startDateStruct":71,"completionDateStruct":73,"leadSponsor":75,"locationsCount":78},"100630914","feasibility-and-ergonomic-impact-of-a-virtual-reality-headset-in-endoscopic-procedures-100630914","NCT07493863","Feasibility and Ergonomic Impact of A Virtual Reality Headset in Endoscopic Procedures","Inclusion Criteria:\n\n* Endoscopist: endoscopist at Cleveland Clinic Weston who consent to participate in the study and are performing either colonoscopy, EUS, or ERCP.\n* Patient: patient undergoing colonoscopy, EUS, or ERCP\n\nExclusion Criteria:\n\n* Exclude the following procedures: Device-assisted colonoscopy (e.g.- double balloon, pathfinder, etc)\n* ERCP in native papilla\n* Cholangioscopy\n* Therapeutic EUS procedures (FNA\u002FFNB, Stent Placement)\n* Planned Mucosal Resection of Polyps \\> 20 mm\n* Inpatient procedures\n* Aborted procedures",true,{"count":55,"type":21},140,[24],"The purpose of this study is to assess the feasibility of using a virtual reality headset (VRH) during endoscopy and its impact on the endoscopist ergonomics. We will use the Apple Vision Pro during approximately 140 endoscopic procedures during which ergonomics will be assessed.",[59,60,61,28],"Ergonomics","Virtual Reality Headset","Virtual Reality",[63,64,65,66],"ergonomics","virtual reality","virtual reality headset","endoscopy","RECRUITING","2026-03-20",{"date":70,"type":39},"2026-03-25",{"date":72,"type":39},"2026-03-10",{"date":74,"type":21},"2026-12",{"name":76,"class":77},"The Cleveland Clinic","OTHER",1,{"id":80,"slug":81,"hasResults":11,"nctId":82,"briefTitle":83,"officialTitle":83,"acronym":4,"eligibilityCriteria":84,"healthyVolunteers":11,"sex":16,"minAge":4,"maxAge":17,"enrollmentInfo":85,"targetDuration":87,"studyType":88,"phases":4,"briefSummary":89,"conditions":90,"keywords":96,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":101,"lastUpdatePostDateStruct":102,"startDateStruct":104,"completionDateStruct":106,"leadSponsor":108,"locationsCount":78},"100602285","airway-complications-in-pediatric-patients-with-tracheostomies-to-what-extent-can-symptoms-identified-by-caregivers-or-pediatricians-serve-as-predictors-for-airway-complications-confirmed-through-surveillance-endoscopy-100602285","NCT07121517","\"Airway Complications in Pediatric Patients With Tracheostomies: To What Extent Can Symptoms Identified by Caregivers or Pediatricians Serve as Predictors for Airway Complications Confirmed Through Surveillance Endoscopy?\"","Inclusion Criteria:\n\nAll children, with tracheostomy, under the age of 18, undergoing scheduled surveillance airway endoscopy in anaesthesia as part of their regular follow-up at the Long term Intensive Care unit (LIVA) at Karolinska University Hospital are eligible for inclusion. Patients may be included several times during the study period.\n\nExclusion criteria:\n\nAll patients undergoing airway endoscopy that is not part of the surveillance airway endoscopy program will be excluded. Thus, emergency endoscopies are not included in this study.",{"count":86,"type":21},100,"2 Years","OBSERVATIONAL","Study Objective:\n\nThis observational study aims to prospectively investigate to what extent tracheostomy-related complications in children are asymptomatic or associated with symptoms when detected through surveillance airway endoscopy. We also aim at investigating how reliable caregiver reports and investigations by pediatriscians are in identifying symptoms associated with severe tracheostomy-related airway complications.\n\nStudy Population:\n\nThe study population comprises children under 18 years of age undergoing follow-up at the Long-Term Intensive Care Unit (LIVA) at Karolinska University Hospital in Stockholm, Sweden.\n\nResearch Questions:\n\n1. To what extent are tracheostomy-related complications in children asymptomatic when detected through surveillance airway endoscopy?\n2. How reliable are caregiver reports in identifying symptoms associated with tracheostomy-related airway complications?\n\nMethods:\n\nChildren scheduled for surveillance airway endoscopy are admitted to LIVA. Upon admission, the caregiver is asked to complete a short questionnaire regarding symptoms that may indicate a tracheostomy-related complication.\n\nAfter the questionnaire has been completed, the child will be examined by the responsible paediatrician, with the aim of identifying any signs or symptoms that could indicate an airway complication. The examination includes physical examination and medical history conducted according to a predefined protocol.\n\nThe airway endoscopy is performed by an ENT surgeon who has not examined the patient beforehand and is not informed of the caregiver's responses nor the result of the examination by the pediatrician. However, there is no strict protocol in place to blind the surgeon to any visibly apparent symptoms or to information that may be spontaneously reported by the caregiver or paediatrician.",[91,28,92,93,94,95],"Surveillance","Tracheostomy Complication","Tracheostomy Complications","Tracheostomy","Children in the Pediatric Intensive Care Unit or General Pediatric Care Unit Requiring a Central Venous Catheter",[97,66,98,99,100],"surveillance","pediatric","intensive care unit","tracheostomy complication","2026-02-12",{"date":103,"type":39},"2026-02-17",{"date":105,"type":39},"2025-09-01",{"date":107,"type":21},"2027-08-31",{"name":109,"class":77},"Karolinska Institutet",{"id":111,"slug":112,"hasResults":11,"nctId":113,"briefTitle":114,"officialTitle":115,"acronym":4,"eligibilityCriteria":116,"healthyVolunteers":11,"sex":16,"minAge":4,"maxAge":4,"enrollmentInfo":117,"targetDuration":4,"studyType":88,"phases":4,"briefSummary":119,"conditions":120,"keywords":4,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":122,"lastUpdatePostDateStruct":123,"startDateStruct":125,"completionDateStruct":127,"leadSponsor":129,"locationsCount":78},"100621937","endoscopy-immersion-study-100621937","NCT07377110","Endoscopy Immersion Study.","Understanding the Impact of Endoscopy Immersion Training in Regional Endoscopy Academies: is it Value for Money?","Inclusion Criteria:\n\nEndoscopy trainees (Surgical, Gastroenterology or CE) who have received (or are soon to undertake) immersion training in either gastroscopy or colonoscopy",{"count":118,"type":21},200,"Endoscopy services are under significant pressure and endoscopy training academies and immersion training are under review at a national level. To date, there has been no comprehensive evaluation of the different approaches to immersion training or a large-scale study looking at its impact on trainees and\u002For endoscopy services. The purpose of this study is to perform a process, impact and economic evaluation of current immersion training practices to determine if they are impactful and value for money.",[121,28],"Training","2026-01-22",{"date":124,"type":39},"2026-01-29",{"date":126,"type":39},"2025-09-09",{"date":128,"type":21},"2026-02",{"name":130,"class":77},"Gloucestershire Hospitals NHS Foundation Trust",{"id":132,"slug":133,"hasResults":11,"nctId":134,"briefTitle":135,"officialTitle":135,"acronym":4,"eligibilityCriteria":136,"healthyVolunteers":11,"sex":16,"minAge":137,"maxAge":138,"enrollmentInfo":139,"targetDuration":4,"studyType":88,"phases":4,"briefSummary":141,"conditions":142,"keywords":4,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":145,"lastUpdatePostDateStruct":146,"startDateStruct":148,"completionDateStruct":150,"leadSponsor":152,"locationsCount":154},"100612762","artificial-intelligence-in-assessing-gastric-intestinal-metaplasia-via-the-eggim-score-100612762","NCT07257796","Artificial Intelligence in Assessing Gastric Intestinal Metaplasia Via the EGGIM Score","Inclusion Criteria:\n\n* patients aged 40-75 years who undergo the IEE examination\n* patients who voluntarily sign the informed consent form\n\nExclusion Criteria:\n\n* patients with severe cardiac, cerebral, pulmonary or renal dysfunction or psychiatric disorders who cannot participate in gastroscopy\n* patients with previous surgical procedures on the stomach","40 Years","75 Years",{"count":140,"type":21},3000,"The endoscopic grading system (EGGIM) has been widely used to assess the extent of gastric intestinal metaplasia during endoscopy. Investigators developed an artificial intelligence (AI) system to automatically evaluate the extent of gastric intestinal metaplasia (GIM) and calculate the EGGIM scores in endoscopy examination. This study is a prospective, multi-center study aimed at exploring the performance and reliability of AI-EGGIM scoring.\n\nThis is a prospective study designed to validate the AI-EGGIM system in a larger cohort. The study protocol was developed based on preliminary experience from a prior investigation (NCT05464108).",[143,144,28],"Intestinal Metaplasia of Gastric Mucosa","Artificial Intelligence","2025-11-27",{"date":147,"type":39},"2025-12-02",{"date":149,"type":39},"2025-11-01",{"date":151,"type":21},"2027-12-31",{"name":153,"class":77},"Qilu Hospital of Shandong University",3,{"id":156,"slug":157,"hasResults":11,"nctId":158,"briefTitle":159,"officialTitle":159,"acronym":160,"eligibilityCriteria":161,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":162,"targetDuration":4,"studyType":22,"phases":164,"briefSummary":165,"conditions":166,"keywords":169,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":172,"lastUpdatePostDateStruct":173,"startDateStruct":175,"completionDateStruct":177,"leadSponsor":179,"locationsCount":78},"100613574","is-cap-assisted-endoscopy-useful-in-acute-upper-gastrointestinal-bleeding--100613574","NCT07268365","Is Cap Assisted Endoscopy Useful in Acute Upper Gastrointestinal Bleeding ?","CAP","Inclusion Criteria:\n\n* Patient \\> 18 years old\n* Upper GI bleeding suspected in presence of melena or hematemesis\n* Glasgow Blatchford score \\> 8\n* Upper gastroscopy at Amiens University Hospital\n* Follow-up at Amiens university hospital\n* Presence of gastric or duodenal ulcer requiring endoscopic hemostasis (FORREST Ia, Ib, IIa, IIb)\n* No opposition to the study\n* No guardianship or curators\n\nExclusion Criteria:\n\n* Patient with clinical suspicion of portal hypertension\n* Known liver failure\n* Patient with digestive hemorrhage related to a lesion located beyond the 2nd duodenum\n* Patient with digestive hemorrhage related to a varicose lesion (esophageal or gastric varices)\n* Patient with bleeding associated with esophagitis\n* Patient with bleeding associated with angiodysplasias",{"count":163,"type":21},72,[24],"High digestive bleeding (HDH) is a medical emergency associated with high morbidity and mortality rates and significant healthcare costs. Upper endoscopy can locate the bleeding and treat it. However, the source of bleeding can be difficult to identify, even for the most experienced endoscopists, due to the location of the bleeding (posterior wall of the bulb, gastric or duodenal folds, papillary region, esophagogastric junction), instability of the tube due to gastric and pyloric contractions and respiratory movements, leading to longer procedure times, hemostasis failure, or even the absence of bleeding visualization. The use of a cap attached to the endoscope facilitates exploration of blind areas of the colonic mucosa located behind folds, thus reducing the rate of missed polyps and cecal intubation time. To date, there is no study evaluating the systematic use of a cap in patients with suspected high digestive bleeding. A series of four cases demonstrated its benefit, allowing for better exposure of the bleeding lesion, better unfolding of intestinal folds, and thus a more effective and quicker hemostatic treatment.",[167,168,28],"Cap-assisted Endoscopy","Upper Gastro Intestinal Bleeding",[170,171,66],"Cap-assisted endoscopy","upper gastro intestinal bleeding","2025-11-25",{"date":174,"type":39},"2025-12-05",{"date":176,"type":39},"2025-10-16",{"date":178,"type":21},"2026-11",{"name":180,"class":77},"Centre Hospitalier Universitaire, Amiens",{"id":182,"slug":183,"hasResults":11,"nctId":184,"briefTitle":185,"officialTitle":185,"acronym":186,"eligibilityCriteria":187,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":138,"enrollmentInfo":188,"targetDuration":4,"studyType":88,"phases":4,"briefSummary":190,"conditions":191,"keywords":195,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":196,"lastUpdatePostDateStruct":197,"startDateStruct":199,"completionDateStruct":201,"leadSponsor":203,"locationsCount":78},"100424601","comparation-of-endoscopic-biopsy-and-postoperative-specimen-for-the-molecular-diagnosis-of-gastric-cancer-100424601","NCT04809025","Comparation of Endoscopic Biopsy and Postoperative Specimen for the Molecular Diagnosis of Gastric Cancer","EBPS","Inclusion Criteria:\n\n1. Lower age limit of research subjects 18 years old and upper age limit of 75 years old.\n2. Histologically proven primary gastric adenocarcinoma (Diagnostic biopsies must be collected within 12 months prior to enrollment).\n3. Written informed consent from the patient.\n4. Patients planned for radical R0 gastrectomy.\n\nExclusion Criteria:\n\n1. Female in pregnancy or lactation.\n2. Patients with gastric cancer who can not undergo tumor resection\n3. Suffering from other serious diseases, including cardiovascular, respiratory, kidney, or liver disease, complicated by poorly controlled hypertension, diabetes, mental disorders or diseases.\n4. Patients with poor compliance or considered to be poor compliance.\n5. Patients received any anticancer drugs, biotherapy, radiotherapy or immunotherapy within 4 weeks before or after enrollment.\n6. Patients after organ transplantation, long-term need to take immunosuppressants, autoimmune diseases.",{"count":189,"type":21},510,"This study aims to test the hypothesis that the diagnosis for histological type, histological grade, LAUREN type, HER-2 expression, MSI\u002FdMMR status, and EBV status in gastric cancer is at least as reliable when performed on endoscopic biopsy specimens as on surgical resection specimens.",[192,28,193,194],"Stomach Neoplasms","Biopsy","Pathology",[192,28,193,194],"2025-09-24",{"date":198,"type":39},"2025-09-29",{"date":200,"type":39},"2021-05-24",{"date":202,"type":21},"2026-09-01",{"name":204,"class":77},"Fudan University",{"id":206,"slug":207,"hasResults":11,"nctId":208,"briefTitle":209,"officialTitle":210,"acronym":4,"eligibilityCriteria":211,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":212,"targetDuration":4,"studyType":22,"phases":214,"briefSummary":215,"conditions":216,"keywords":4,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":225,"lastUpdatePostDateStruct":226,"startDateStruct":228,"completionDateStruct":230,"leadSponsor":232,"locationsCount":78},"100590208","raman-spectroscopy-in-the-diagnosis-of-extrahepatic-cholangiocarcinoma---a-pilot-study-100590208","NCT06964425","Raman Spectroscopy in the Diagnosis of Extrahepatic Cholangiocarcinoma - a Pilot Study","Raman Spectroscopy in the Diagnosis of Extrahepatic Cholangiocarcinoma","Inclusion Criteria:\n\n* person older than 18 years, who has known extrahepatic cholangiocarcinoma and is indicated for ERCP\n\nExclusion Criteria:\n\n* disagreement with the study",{"count":213,"type":21},20,[24],"Diagnosis of extrahepatic cholangiocarcinoma is challenging because the yield of imaging and tissue sampling is limited. Raman spectroscopy is an optical method based on the analysis of scattered monochromatic light. Raman spectroscopy is able to provide a molecular 'fingerprint' of the tissue to determine its type. The aim of this pilot study was to develop a methodology for in vivo Raman spectroscopy in bile ducts to improve the current diagnostic capabilities of extrahepatic cholangiocarcinoma.",[217,218,219,220,221,222,28,223,224],"Cholangiocarcinoma, Extrahepatic","Cholangiocarcinoma of the Extrahepatic Bile Duct","Cholangiocarcinoma, Perihilar","Diagnosis","Raman Spectroscopy","Klatskin Tumor","Biliary Stricture","Malignant Biliary Stricture","2025-06-29",{"date":227,"type":39},"2025-07-02",{"date":229,"type":39},"2023-02-04",{"date":231,"type":21},"2025-07-30",{"name":233,"class":77},"University Hospital Olomouc",{"id":235,"slug":236,"hasResults":11,"nctId":237,"briefTitle":238,"officialTitle":238,"acronym":239,"eligibilityCriteria":240,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":241,"targetDuration":4,"studyType":22,"phases":243,"briefSummary":244,"conditions":245,"keywords":246,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":248,"lastUpdatePostDateStruct":249,"startDateStruct":251,"completionDateStruct":253,"leadSponsor":255,"locationsCount":4},"100592906","use-of-virtual-reality-technologies-in-management-of-anxiety-and-discomfort-during-endoscopy-procedure-100592906","NCT06999525","Use of Virtual Reality Technologies in Management of Anxiety and Discomfort During Endoscopy Procedure","CARVENDO","Inclusion Criteria:\n\n* Age ≥ 18 years (adult patients)\n* Affiliated with a French social security system\n* No legal protection measures (e.g., guardianship, curatorship)\n* Scheduled for outpatient digestive endoscopy (upper or lower) under general anesthesia, level 1 (excluding biliary or interventional procedures)\n* Medical indication for the endoscopic procedure established by a clinician\n\nExclusion Criteria:\n\n* History of epilepsy\n* Claustrophobia",{"count":242,"type":21},50,[24],"Digestive endoscopies are performed either for diagnostic purposes (e.g. suspicion of cancer or monitoring of chronic diseases) or for therapeutic purposes (treatment of digestive haemorrhage, removal of polyps, etc.).\n\nSome endoscopies are performed under local anaesthetic, which can cause considerable anxiety in anticipation of the procedure and considerable discomfort during the procedure. Other endoscopies are performed under general anaesthetic for more extensive procedures on outpatients or inpatients. Anxiety prior to anaesthesia is likely to increase the perception of pain, increase the need for anaesthetic products and thus increase the time to complete awakening.\n\nComplementary techniques such as hypnotherapy can be used before the operation, with proven effectiveness. But these techniques require dedicated and specifically trained staff, as well as additional time.\n\nVirtual reality technologies, and in particular virtual reality headsets, allow instant immersion in a relaxing world. Therapeutic virtual reality headsets (TRVH) have been shown to be effective in reducing pre-operative anxiety and pain perception.\n\nOur hypothesis is that the use of a CRVT could reduce the consumption of anaesthetic products, reduce anxiety, improve overall satisfaction and reduce the length of outpatient hospitalisation during digestive endoscopy procedures.",[28],[28,247],"Virtual reality technologies","2025-05-30",{"date":250,"type":39},"2025-05-31",{"date":252,"type":21},"2025-07",{"date":254,"type":21},"2027-01",{"name":256,"class":77},"Assistance Publique - Hôpitaux de Paris",{"id":258,"slug":259,"hasResults":11,"nctId":260,"briefTitle":261,"officialTitle":261,"acronym":262,"eligibilityCriteria":263,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":264,"targetDuration":266,"studyType":88,"phases":4,"briefSummary":267,"conditions":268,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":270,"lastUpdatePostDateStruct":271,"startDateStruct":273,"completionDateStruct":275,"leadSponsor":277,"locationsCount":279},"100561416","french-prospective-cohort-of-innovative-endoscopic-interventions-in-expert-centers-100561416","NCT06589882","French Prospective Cohort of Innovative Endoscopic Interventions in Expert Centers","CoPPInE","Inclusion Criteria:\n\n* Patients \\> 18 yo\n* Patient able to give consent\n* Patient with innovative endoscopy\n\nExclusion Criteria:\n\n* Opposition to participation in the present project to be notified in the file\n* Patient under court protection",{"count":265,"type":21},10000,"10 Years","The creation of a multi-center French cohort pooling data from innovative endoscopies carried out in France every year would make it possible to produce excellent scientific results and analyze on a large scale the results of our current practices.",[28,269],"Innovative Procedures","2024-09-06",{"date":272,"type":39},"2024-09-19",{"date":274,"type":21},"2024-10-01",{"date":276,"type":21},"2034-09-01",{"name":278,"class":77},"Centre Hospitalier Universitaire de Nīmes",2,{"id":281,"slug":282,"hasResults":11,"nctId":283,"briefTitle":284,"officialTitle":284,"acronym":4,"eligibilityCriteria":285,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":286,"targetDuration":4,"studyType":88,"phases":4,"briefSummary":287,"conditions":288,"keywords":289,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":292,"lastUpdatePostDateStruct":293,"startDateStruct":294,"completionDateStruct":296,"leadSponsor":298,"locationsCount":78},"100552041","prospective-collection-of-endoscopic-and-histopathologic-data-from-endoscopic-procedures-performed-in-uz-gent-100552041","NCT06467929","Prospective Collection of Endoscopic and Histopathologic Data from Endoscopic Procedures Performed in UZ Gent","Inclusion Criteria:\n\n* Age =\\> 18 years\n* Referral for a surveillance, diagnostic or therapeutic endoscopy\n* Digital video material of the endoscopic procedure\n* Digital images of the endoscopic procedure\n* Videos and\u002For images can be made in white light or any virtual of dye-based enhancement technique\n* Endoscopic procedures performed after IRB approval for this study\n* Material collected in adult patients of all sex or race, including pregnant women\n\nExclusion Criteria:\n\n* Age \\\u003C 18 years\n* Any contraindication to undergo an endoscopic procedure\n* Patient did not sign informed consent",{"count":189,"type":21},"This is an observational study in which images (photos and\u002For videos of lesions found during endoscopy) will be collected and the associated data about these lesions (size, location in the body, outcome of histology, if resected and examined).\n\nThe images will be taken while performing a diagnostic or therapeutic endoscopy. This footage can be recorded in different light modalities, and various lesions can be removed during one procedure. It is of importance that the images are recorded in the best possible image quality.\n\nThe images can be either endoscopic images or endoscopic images combined with room view (this means that the endoscopic room can be filmed, for example, to visualize the endoscopist and thus show techniques of the procedure, without the patient being identified). The GDPR regulations will be respected at all times during the video recordings.\n\nThe purpose of this registry is to create a database with images in the form of photos and video clips, histopathological data, demographic data of patients and data about the endoscopic procedure. The recording of this data is standard with every endoscopic procedure that patients undergo at UZ Gent.\n\nThe data will be used for the following purposes: linking procedural outcomes with procedural data and patient data to improve endoscopic technique and to guarantee quality in our endoscopic unit. In this way the investigators will also be able to identify trends and link adverse events back to the patient data with the aim of informing the patient. In addition, as a university center, the investigators can train doctors in training with this educational material. The footage can be shared via online and\u002For live presentations that are only accessible to\u002Fby healthcare workers and without the patient being identifiable. Such material and its dissemination is essential to improve (the safety of) techniques (such as those of today), to share knowledge about techniques, and in this way to train the next generation of doctors and nurses.",[28],[66,290,291],"histopathology","database","2024-09-05",{"date":272,"type":39},{"date":295,"type":39},"2022-12-22",{"date":297,"type":21},"2025-10-30",{"name":299,"class":77},"University Hospital, Ghent"]