[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"training\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:training":24},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,10,0,[8,38,75,97,123,144,172,201,237,265],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":17,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":22,"conditions":23,"keywords":4,"overallStatus":25,"whyStopped":4,"lastUpdateSubmitDate":26,"lastUpdatePostDateStruct":27,"startDateStruct":30,"completionDateStruct":32,"leadSponsor":34,"locationsCount":37},"100645092","feasibility-of-point-of-care-ultrasound-training-and-remote-quality-assurance-for-community-physicians-in-conflict-affected-syria-100645092",false,"NCT07677553","Feasibility of Point-of-Care Ultrasound Training and Remote Quality Assurance for Community Physicians in Conflict-Affected Syria","Inclusion Criteria:Nine physicians from five community clinics serving villages in a region of Syria that cannot be further specified for security reasons participated in the program. Participants represented several medical specialties and were selected in collaboration with IFA based on their involvement in frontline community care and their anticipated ability to integrate POCUS into clinical practice.\n\n\\-\n\nExclusion Criteria:None\n\n\\-","ALL","18 Years","99 Years",{"count":19,"type":20},9,"ESTIMATED","OBSERVATIONAL","Background: POCUS can extend diagnostic capabilities where conventional imaging is unavailable, yet evidence on its implementation in active conflict zones remains scarce. We describe the feasibility of a POCUS training, device deployment, and remote quality assurance program for community physicians working in village clinics in Syria.\n\nMethods: Nine physicians from five community clinics participated in a two-day in-person POCUS training course adapted to a conflict-affected, resource-constrained setting. The curriculum focused on cardiac, lung, FAST, and soft-tissue applications. At course completion, each clinic received a handheld Butterfly ultrasound device. Participants subsequently uploaded examinations to a cloud-based platform for remote expert review and feedback. Outcomes included immediate post-course satisfaction, perceived confidence, and early post-course POCUS use over follow-up.",[24],"Training","RECRUITING","2026-06-24",{"date":28,"type":29},"2026-07-01","ACTUAL",{"date":31,"type":29},"2026-01-01",{"date":33,"type":20},"2026-08-31",{"name":35,"class":36},"Meir Medical Center","OTHER",1,{"id":39,"slug":40,"hasResults":11,"nctId":41,"briefTitle":42,"officialTitle":43,"acronym":4,"eligibilityCriteria":44,"healthyVolunteers":45,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":46,"targetDuration":4,"studyType":48,"phases":49,"briefSummary":51,"conditions":52,"keywords":60,"overallStatus":65,"whyStopped":4,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":67,"startDateStruct":69,"completionDateStruct":71,"leadSponsor":73,"locationsCount":4},"100642365","caregiver-training-regarding-percutaneous-endoscopic-gastrostomy-feeding-and-care-100642365","NCT07647185","Caregiver Training Regarding Percutaneous Endoscopic Gastrostomy Feeding and Care","Effects of Caregiver Training on Stress, Knowledge, and Skill Level Regarding Percutaneous Endoscopic Gastrostomy Care","Inclusion Criteria:\n\n* Being 18 years of age or older\n* Being the patient's primary caregiver (the person who regularly provides daily PEG care and nutrition)\n* Being literate\n* Being proficient in communicating in Turkish (understanding and expressing oneself)\n* Volunteering to participate in the study and providing written informed consent\n* The caregiver must not have a diagnosed psychiatric illness requiring active treatment\n\nExclusion Criteria:\n\n* Being under 18 years of age\n* Being illiterate\n* Not being proficient in communicating in Turkish\n* Not giving written informed consent to participate in the study\n* Having a diagnosed psychiatric illness requiring active treatment",true,{"count":47,"type":20},54,"INTERVENTIONAL",[50],"NA","Background: Percutaneous endoscopic gastrostomy (PEG) is used for patients who cannot be fed orally, have a reduced swallowing reflex, or require long-term feeding. PEG care and feeding, which is performed with nursing support in healthcare institutions, becomes the responsibility of the caregiver after discharge. During this process, a lack of information and insufficient mastery of PEG feeding can create stress for caregivers. This situation jeopardizes patient safety. Therefore, healthcare professionals should manage patient-centered care from the moment the PEG indication is established until discharge. In this regard, consistent guidance and healthcare education are needed for caregivers.\n\nAim and hypotheses: This study aims to examine the effects of hands-on PEG feeding and PEG care training, enriched with audiovisual materials (video), on caregivers' knowledge level, skills, and stress levels related to the PEG feeding and care process.\n\nH1: The training provided for caregivers increases their knowledge level regarding PEG feeding and care.\n\nH2: The training provided for caregivers increases their skill level regarding PEG feeding and care.\n\nH3: The training provided for caregivers reduces their stress levels related to PEG feeding and care.\n\nDesign: This study was designed as a randomized controlled trial with experimental and control groups.\n\nMethod: The study population will consist of caregivers of patients receiving inpatient care at a state hospital and undergoing PEG placement for the first time. The sample size was calculated using the G-Power 3.1 program, resulting in a sample size of 54 (n1=27, n2=27), including the dropout rate. Participants will be randomly assigned to groups. The intervention group will receive hands-on training related to PEG feding and care using a low-fidelity model. In addition, caregivers will be provided with video training on PEG feeding and care that they can watch for review when needed. The control group will receive standard institutional training provided by the nutrition nurse of the institution where the study is conducted. Data will be collected face-to-face using a \"Personal Information Form\", \"State Anxiety Inventory\", \"Skills Checklist\", and \"PEG Care Konowledge Form\". Three measurements will be taken in the study. Test 0: Before the training (Personal Information Form, State Anxiety Inventory), Test 1: After the training (with the PEG Care Knowledge Form and the State Anxiety Inventory). Additionally, the researcher will evaluate the caregiver's feeding and care practices using the Skills Checklist. Test 2: Two weeks after from the Test 1 (State Anxiety Inventory and PEG Care Konowledge Form), also the researcher will also evaluate the caregiver's practices a second time using the Skills Checklist. Data will be analyzed using the SPSS Statistics 27 software package.",[53,54,55,56,57,58,59,24],"Caregiver","Caregiver Anxiety","Simulation Training","State Anxiety","Nursing Care","Video-Assisted","Percutaneous Endoscopic Gastrostomy (PEG)",[61,62,55,63,64],"Nursing","Caregivers","Anxiety","Gastrostomy","NOT_YET_RECRUITING","2026-06-09",{"date":68,"type":29},"2026-06-15",{"date":70,"type":20},"2026-08-01",{"date":72,"type":20},"2027-03-30",{"name":74,"class":36},"Duzce University",{"id":76,"slug":77,"hasResults":11,"nctId":78,"briefTitle":79,"officialTitle":80,"acronym":4,"eligibilityCriteria":81,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":82,"targetDuration":4,"studyType":48,"phases":84,"briefSummary":85,"conditions":86,"keywords":4,"overallStatus":25,"whyStopped":4,"lastUpdateSubmitDate":88,"lastUpdatePostDateStruct":89,"startDateStruct":91,"completionDateStruct":93,"leadSponsor":95,"locationsCount":37},"100569162","self-practicing-upper-body-exercises-with-a-robotic-trainer-system-100569162","NCT06690658","Self-Practicing Upper Body Exercises With a Robotic Trainer System","Self-Practicing Upper Body Exercises With a Robotic Trainer System in the Physical Therapy Department: A Feasibility Study","Inclusion Criteria:\n\n* 18 years ≤ Age\n* stable clinical and metabolic state\n* ability to sit without back support independently\n* ability to understand research instructions.\n\nExclusion Criteria:\n\n* A contraindication to perform active upper extremity movements\n* Severe pain that limits the ability to exercise.",{"count":83,"type":20},30,[50],"Studies suggest that older adults undergoing inpatient rehabilitation have relatively low levels of physical activity. Moreover, people with lower limb orthopedic conditions undergoing inpatient rehabilitation may be particularly vulnerable to the consequences of low physical activity because of the mobility limitations.\n\nThe study focuses on examining the feasibility of incorporating robotic system for upper body physical training of people with lower limb orthopedic condition undergoing inpatient rehabilitation. Using robotic coaches can be a complementary method to promote the participation and motivation of people with lower limb orthopedic conditions undergoing inpatient rehabilitation.\n\nAims:\n\nThe overall aim of the study is to assess the user experience and feasibility of incorporating robotic system for upper body physical training of people with lower limb orthopedic injury\u002Fcondition undergoing inpatient rehabilitation. Our specific aims are:\n\n1. To assess the acceptability and suitability of the training (i.e., training attendance and engagement; adherence to training protocol; time on task; satisfaction and enjoyment of the training)\n2. To document unexpected adverse events during training.\n3. To assess the resources and ability to manage and implement the training (i.e., administrative capacity, technology and equipment needs and training).",[87,24],"Robot Assisted Therapy","2026-05-25",{"date":90,"type":29},"2026-05-27",{"date":92,"type":29},"2025-01-21",{"date":94,"type":20},"2027-01",{"name":96,"class":36},"Loewenstein Hospital",{"id":98,"slug":99,"hasResults":11,"nctId":100,"briefTitle":101,"officialTitle":102,"acronym":103,"eligibilityCriteria":104,"healthyVolunteers":45,"sex":15,"minAge":4,"maxAge":4,"enrollmentInfo":105,"targetDuration":4,"studyType":48,"phases":106,"briefSummary":107,"conditions":108,"keywords":4,"overallStatus":65,"whyStopped":4,"lastUpdateSubmitDate":114,"lastUpdatePostDateStruct":115,"startDateStruct":117,"completionDateStruct":119,"leadSponsor":121,"locationsCount":37},"100622612","ultrasound-guided-non-invasive-simulation-in-anesthesia-residency-training-100622612","NCT07385885","Ultrasound-guided Non-invasive Simulation in Anesthesia Residency Training","Application of Ultrasound-guided Non-invasive Simulated Puncture Technique in Standardized Residency Training in Anesthesiology","non-invasive","Inclusion Criteria:\n\n\\~Anesthesiology residents participating in the standardized residency training program in the Department of Anesthesiology at Nanjing First Hospital between October 2024 and October 2026.\n\nExclusion Criteria:\n\n* Residents with prior experience in performing nerve block procedures.\n* Residents currently participating in other teaching or research studies related to nerve blocks.",{"count":83,"type":20},[50],"Study Aim: This trial evaluates if a novel non-invasive, AI-assisted simulation training improves ultrasound-guided needle visualization skills in anesthesia residents.\n\nDesign: Trainees were randomized into two groups:\n\nIntervention: AI-based, non-invasive simulated needle puncture training. Control: Conventional ultrasound teaching. Key Outcomes: The primary outcome is objective needle tip visibility. Secondary outcomes include anatomical identification, correct view acquisition, operator confidence, and overall scanning performance.\n\nAssessment: Outcomes are measured via blinded expert evaluation and theoretical tests.\n\nThe goal of this randomized controlled clinical trial is to determine whether an ultrasound-guided non-invasive simulated needle puncture training technique can improve ultrasound-guided needle visualization skills in anesthesiology residents undergoing standardized residency training. The study is conducted in anesthesiology residents enrolled in a standardized residency training program.\n\nThe main questions it aims to answer are:\n\n1. Does non-invasive simulated needle puncture training improve objective needle tip visibility during ultrasound-guided peripheral nerve block procedures?\n2. Does this training method improve anatomical structure identification, acquisition of correct block views, operator confidence, and overall scanning performance compared with conventional ultrasound teaching? Researchers will compare a non-invasive simulated needle puncture training group with a conventional ultrasound teaching group to see if the simulated training technique leads to superior needle visualization and procedural performance.\n\nParticipants will:\n\nReceive standardized theoretical instruction on ultrasound- guided peripheral nerve blocks; Be randomly assigned to either non-invasive simulated needle puncture training using an artificial intelligence-assisted system or conventional ultrasound scanning training; Perform ultrasound scanning and simulated or conventional practice on healthy volunteers; Undergo theoretical examinations and blinded expert assessments of ultrasound scanning performance and needle visualization outcomes.",[109,110,111,112,24,113],"Ultrasound","Needle","Residency","Anesthesiology","Non-invasive","2026-02-03",{"date":116,"type":29},"2026-02-04",{"date":118,"type":20},"2026-02-01",{"date":120,"type":20},"2028-12-30",{"name":122,"class":36},"Nanjing First Hospital, Nanjing Medical University",{"id":124,"slug":125,"hasResults":11,"nctId":126,"briefTitle":127,"officialTitle":128,"acronym":4,"eligibilityCriteria":129,"healthyVolunteers":11,"sex":15,"minAge":4,"maxAge":4,"enrollmentInfo":130,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":132,"conditions":133,"keywords":4,"overallStatus":25,"whyStopped":4,"lastUpdateSubmitDate":135,"lastUpdatePostDateStruct":136,"startDateStruct":138,"completionDateStruct":140,"leadSponsor":142,"locationsCount":37},"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":131,"type":20},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.",[24,134],"Endoscopy","2026-01-22",{"date":137,"type":29},"2026-01-29",{"date":139,"type":29},"2025-09-09",{"date":141,"type":20},"2026-02",{"name":143,"class":36},"Gloucestershire Hospitals NHS Foundation Trust",{"id":145,"slug":146,"hasResults":11,"nctId":147,"briefTitle":148,"officialTitle":149,"acronym":150,"eligibilityCriteria":151,"healthyVolunteers":45,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":152,"targetDuration":4,"studyType":48,"phases":154,"briefSummary":155,"conditions":156,"keywords":160,"overallStatus":65,"whyStopped":4,"lastUpdateSubmitDate":164,"lastUpdatePostDateStruct":165,"startDateStruct":167,"completionDateStruct":168,"leadSponsor":170,"locationsCount":4},"100598654","training-program-for-peg-caregivers-a-structured-intervention-study-100598654","NCT07074301","Training Program for PEG Caregivers: A Structured Intervention Study","Effectiveness of Education and Mobile Application for Percutaneous Endoscopic Gastrostomy Care","PEG-EDU","Inclusion Criteria:\n\n* Age 18 or older\n* Willingness to participate voluntarily in the study\n* No communication barriers\n* Ability to use a smartphone\n* No diagnosed psychiatric disorder\n* Providing care to a patient aged 18 or older who is scheduled to undergo PEG placement\n\nExclusion Criteria:\n\n* Discharge from hospital or death of the patient during the study period\n* Being under 18 years old\n* Illiteracy of the caregiver",{"count":153,"type":20},80,[50],"This study aims to develop and evaluate a structured education program and a mobile application to support caregivers of patients receiving enteral nutrition via percutaneous endoscopic gastrostomy (PEG). The intervention focuses on improving caregivers' knowledge, care practices, and perceived burden. The study will be conducted in three phases: a needs assessment, development of the education and digital support modules, and implementation of the intervention. Quantitative and qualitative data will be collected to evaluate the impact of the intervention. The results are expected to contribute to the improvement of home PEG care quality and the empowerment of caregivers.",[59,24,157,158,159],"Caregiver Burden","Nutritional Support","Training Effectiveness",[161,157,162,163],"Percutaneous endoscopic gastrostomy","Structured Training","Home Enteral Nutrition","2025-08-29",{"date":166,"type":29},"2025-09-05",{"date":166,"type":20},{"date":169,"type":20},"2026-03-31",{"name":171,"class":36},"Koç University",{"id":173,"slug":174,"hasResults":11,"nctId":175,"briefTitle":176,"officialTitle":177,"acronym":178,"eligibilityCriteria":179,"healthyVolunteers":11,"sex":15,"minAge":4,"maxAge":4,"enrollmentInfo":180,"targetDuration":182,"studyType":21,"phases":4,"briefSummary":183,"conditions":184,"keywords":187,"overallStatus":25,"whyStopped":4,"lastUpdateSubmitDate":191,"lastUpdatePostDateStruct":192,"startDateStruct":194,"completionDateStruct":196,"leadSponsor":198,"locationsCount":200},"100449140","endoscopic-ultrasound-guided-gastroenterostomy-nationwide-prospective-registry-100449140","NCT05128604","Endoscopic Ultrasound-Guided Gastroenterostomy Nationwide: Prospective Registry.","Introduction Of Endoscopic Ultrasound-Guided Gastroenterostomy Based On A Learning Protocol And Prospective Registry.","GESICA","Inclusion Criteria:\n\n* Age 18 years or more\n* Gastric outlet obstruction (GOO) caused by passable \u002Funpassable stenosis in the antrum-duodenal region, to malignant or non-malignant conditions\n* Patient capable of understanding and signing informed consent form\n* Patient understanding the type of study and complying with the follow-up of complementary tests during the study's duration\n\nExclusion Criteria:\n\n* Massive ascites.\n* Complete stenosis\n* Failure to sign informed consent form\n* Patients with intellectual handicap who are unable to understand the nature and possible consequences of the study, unless there is a competent legal representative\n* Patients unable to adhere to subsequent follow-up requirements\n* Severe coagulation disorder: INR \\> 1.5 not correctible with administration of plasma and\u002For platelets \\\u003C 50,000\u002Fmm3",{"count":181,"type":20},50,"6 Months","This is project of help and support for the introduction of the GASTROENTEROANASTOMOSIS technique guided by ENDOSCOPIC -ULTRASOUND (EUS-GE) in centers in Catalonia, facilitating a teacher training.\n\nThe main objective is facilitate a safe introduction of the technique, limiting technical failures, and if necessary, support in rescue techniques.\n\nThe goal of this interventional study is to assess the impact of a teaching and on live-support model in the introduction of the gastroenteroanastomosis technique, evaluating its effects in safety and the learning curve.\n\nregarding the results in safety and learning curve of for the introduction \\[type of study: observational study or clinical trial\\] is to \\[learn about, test, compare etc.\\] in \\[describe participant population\u002Fhealth conditions\\]. The main question\\[s\\] it aims to answer are:\n\n* \\[question 1\\]\n* \\[question 2\\] Participants will \\[describe the main tasks participants will be asked to do, treatments they'll be given and use bullets if it is more than 2 items\\]. If there is a comparison group: Researchers will compare \\[insert groups\\] to see if \\[insert effects\\].",[185,186,24],"Endoscopic Surgical Procedure","Safety",[188,189,190],"endoscopic ultrasound","gastroenterostomy","lumen apposing stent","2025-07-25",{"date":193,"type":29},"2025-07-29",{"date":195,"type":29},"2022-05-23",{"date":197,"type":20},"2026-09-24",{"name":199,"class":36},"Hospital Universitari de Bellvitge",6,{"id":202,"slug":203,"hasResults":11,"nctId":204,"briefTitle":205,"officialTitle":206,"acronym":4,"eligibilityCriteria":207,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":208,"targetDuration":4,"studyType":48,"phases":210,"briefSummary":211,"conditions":212,"keywords":222,"overallStatus":65,"whyStopped":4,"lastUpdateSubmitDate":229,"lastUpdatePostDateStruct":230,"startDateStruct":232,"completionDateStruct":234,"leadSponsor":235,"locationsCount":37},"100591839","khanya-ekhaya-a-home-based-intervention-100591839","NCT06985641","Khanya Ekhaya: A Home-Based Intervention","Home-Based Community Health Worker Support for Mental Health Among People Living With HIV in South Africa: A Hybrid Effectiveness Implementation Trial","Inclusion Criteria:\n\nCHWs:\n\n* at least 18 years old\n* must conduct home visits for people with HIV newly initiating or re-initiating ART at the approved clinic site\n\nPATIENTS:\n\n* at least 18 years old\n* seen by a CHW after newly initiating or re-initiating ART in the past three months\n* screen positive for depressive symptoms or harmful alcohol use\n\nExclusion Criteria:\n\nCHWs:\n\n-Unable or unwilling to complete informed consent and study procedures in English, isiXhosa, or Afrikaans\n\nPATIENTS:\n\n-Unable or unwilling to complete informed consent and study procedures in English, isiXhosa, or Afrikaans",{"count":209,"type":20},119,[50],"Mental health conditions, such as depression, anxiety, and harmful alcohol use are prevalent among people with chronic diseases, including HIV, and contribute to poor engagement in care. There is a need to address untreated mental health problems. Community health workers (CHWs) are frontline workers who play a central role in supporting vulnerable individuals to stay in care, including seeking people living with HIV who are newly initiating antiretroviral therapy (ART) or re-initiating after a period of care disengagement. CHW-delivered interventions are promising for improving engagement and retention in care. Yet, these programs rarely address mental health -a significant barrier to chronic disease care engagement and treatment. An approach that moves beyond providing care in the clinic setting is needed. Community-delivered home-based mental health care has been shown to be feasible and acceptable and shows promise for integration into broader community health care services for people with chronic conditions, such as HIV.",[213,214,215,216,217,218,24,219,220,221],"HIV","HIV Antiretroviral Therapy (ART) Adherence","Mental Health","Substance Use Disorders","Stigma","Community Health Workers","Global Health","Mental Health Recovery","Substance Use Recovery",[218,223,219,221,220,213,224,225,226,227,228,216],"Health Personnel","Health Care Seeking Behavior","Treatment Adherence and Compliance","Attitude of Health Personnel","Substance Use Stigma","Mental health Stigma","2025-05-14",{"date":231,"type":29},"2025-05-22",{"date":233,"type":20},"2025-09-01",{"date":68,"type":20},{"name":236,"class":36},"University of Maryland, College Park",{"id":238,"slug":239,"hasResults":11,"nctId":240,"briefTitle":241,"officialTitle":242,"acronym":243,"eligibilityCriteria":244,"healthyVolunteers":11,"sex":15,"minAge":4,"maxAge":4,"enrollmentInfo":245,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":247,"conditions":248,"keywords":251,"overallStatus":65,"whyStopped":4,"lastUpdateSubmitDate":257,"lastUpdatePostDateStruct":258,"startDateStruct":260,"completionDateStruct":261,"leadSponsor":263,"locationsCount":37},"100586904","evaluating-decision-making-using-chatgpt-4-among-trainees-in-surgery-100586904","NCT06921447","Evaluating Decision-making Using ChatGPT-4 Among Trainees in Surgery","Evaluating ChatGPT-4 as a Decision-Making Support Tool for Surgical Trainees","EDuCATe","Inclusion Criteria:\n\n* Actively enrolled or employed in the general surgery residency or department at the participating institution\n* Willingness to participate and complete all clinical case scenarios\n* Consent to participate in the study\n\nExclusion Criteria:\n\n* Incomplete responses\n* Use of external assistance (e.g., internet search, AI tools) when answering scenarios, as self-reported in instructions",{"count":246,"type":20},35,"This study aims to assess whether ChatGPT-4 can support surgical trainees in clinical decision-making. By comparing the performance of ChatGPT-4 with junior residents, senior residents, and attending surgeons on standardized clinical scenarios, the study seeks to understand the potential role of large language models in surgical education. The ultimate goal is to evaluate whether ChatGPT-4 can be safely integrated as a supplementary educational tool to aid junior residents in developing critical thinking and surgical judgment.",[249,24,250],"Artificial Intelligence (AI)","Surgery",[252,253,254,255,256],"artificial intelligence","surgery","training","oncology","emergency","2025-04-08",{"date":259,"type":29},"2025-04-10",{"date":259,"type":20},{"date":262,"type":20},"2025-04-30",{"name":264,"class":36},"Ospedali Riuniti Trieste",{"id":266,"slug":267,"hasResults":11,"nctId":268,"briefTitle":269,"officialTitle":270,"acronym":271,"eligibilityCriteria":272,"healthyVolunteers":45,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":273,"targetDuration":4,"studyType":48,"phases":275,"briefSummary":276,"conditions":277,"keywords":4,"overallStatus":65,"whyStopped":4,"lastUpdateSubmitDate":285,"lastUpdatePostDateStruct":286,"startDateStruct":288,"completionDateStruct":290,"leadSponsor":292,"locationsCount":37},"100430774","standardizing-right-hemicolectomy-for-colon-cancer-100430774","NCT04889456","Standardizing Right Hemicolectomy for Colon Cancer","Implementation of Optimized and Standardized Surgical Technique for Right Sided Colon Cancer: a Prospective Interventional Sequential Cohort Study With a Transition Period","Right","Inclusion Criteria:\n\n* Planned laparoscopic (extended) right hemicolectomy for colon cancer of the caecum, ascending colon or hepatic flexure;\n* Age above 18 years;\n* cTNM stage 1-3 (CT-staged);\n* No prior midline or transverse laparotomy;\n* ASA1-3;\n* No immune modulating medication.\n\nExclusion Criteria:\n\n* cT4b;\n* Perforated disease;\n* Acute obstruction;\n* Emergency operation;\n* Appendiceal cancer;\n* Other primary malignancy treated within 5 years from diagnosis of colon cancer, except for curatively treated prostate, breast, skin and cervical cancer.",{"count":274,"type":20},930,[50],"A surgical intervention might be highly variable amongst surgeons and centers. This variability has a potential relevance concerning clinical outcomes.\n\nFor right-sided colon cancer, the laparoscopic right hemicolectomy (LRHC) knows substantial variation. Especially since the surgical technique has been evolving during the latest decade with the introduction of intracorporeal anastomosis, a dissection technique within the correct embryological planes (complete mesocolic excision) and central vascular ligation of the segmental branches at its origin, resulting in an optimal lymph node dissection.\n\nGiven the insights from recent studies showing the association between quality of surgery and relevant clinical outcomes, there is a great need for a formative quality assessment of LRHC. Detailed objective assessment of the LRHC is currently not performed in clinical practice nor in surgical training. Quality assessment of LRHC has great potential to improve surgical training and furthermore, implementation of a standardized technique will ultimately lead to better quality of care for patients suffering from right-sided colon cancer.\n\nThe main objective of this study is to improve surgical outcomes for patient with right-sided colon cancer by a prospective sequential interventional cohort study that aims to standardize the surgical technique with subsequent controlled implementation after standardized review of the current practice in a nationwide multicenter setting. The primary endpoint is the 30-day morbidity according to the Clavien-Dindo classification system.",[278,279,280,24,281,282,283,284],"Colonic Carcinoma","Laparoscopic Right Hemicolectomy","Standardisation","Delphi Study","Implementation","Consolidation","Assessment","2021-05-13",{"date":287,"type":29},"2021-05-17",{"date":289,"type":20},"2021-07-01",{"date":291,"type":20},"2027-07-01",{"name":293,"class":36},"Amsterdam UMC, location VUmc"]