[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"surgical\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:surgical":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,49,82],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":31,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":38,"lastUpdatePostDateStruct":39,"startDateStruct":42,"completionDateStruct":44,"leadSponsor":46,"locationsCount":4},"100618913","implementation-of-clinical-nutrition-practice-guidelines-in-surgical-icus-100618913",false,"NCT07337798","Implementation of Clinical Nutrition Practice Guidelines in Surgical ICUs","Effects of Implementing Evidence-Based Clinical Nutrition Practice Guidelines in Surgical Intensive Care Units: A Cohort Study","Inclusion Criteria:\n\nFor ICU healthcare professionals:\n\nEmployed at one of the participating study sites (tertiary general hospitals)\n\nHolds a valid Registered Nurse license issued in the People's Republic of China\n\nCurrently working in frontline clinical nursing care in a surgical intensive care unit (ICU) during the study period\n\nAt least 1 year of clinical working experience\n\nAble to understand the study objectives and procedures\n\nWilling to participate and able to provide written informed consent\n\nFor surgical critically ill patients (outcome assessment population):\n\nAged 18 years or older\n\nAdmitted to a surgical ICU due to surgical-related conditions, including trauma, infection, malignancy, or postoperative complications\n\nExpected length of stay in the surgical ICU of at least 48 hours\n\nNo restriction on sex\n\nPatient or legally authorized representative able to provide written informed consent\n\nExclusion Criteria:\n\nFor ICU healthcare professionals:\n\nCurrently pregnant, breastfeeding, or planning pregnancy during the study period\n\nTemporarily assigned, rotating, externally dispatched, on long-term training, or on leave during the study period, making continuous participation impossible\n\nParticipation in other interventional studies that may interfere with the implementation of this study\n\nDetermined by the research team to have cognitive, communication, or other conditions that would make participation inappropriate\n\nFor surgical critically ill patients:\n\nDiagnosed with brain death or awaiting organ donation\n\nPregnant or breastfeeding women\n\nConcurrent participation in other nutrition-related clinical trials","ALL","18 Years",{"count":19,"type":20},200,"ESTIMATED","INTERVENTIONAL",[23],"NA","The goal of this interventional clinical trial is to evaluate whether the implementation of an evidence-based, context-adapted clinical nutrition practice guideline can improve clinical nutrition management in surgical intensive care units (ICUs) in China. The guideline is selected based on the best available evidence from existing surgical and critical care nutrition guidelines, adapted to the Chinese healthcare context, and implemented using an i-PARIHS-guided translation strategy. The trial involves ICU healthcare professionals working in surgical ICUs of tertiary general hospitals, while assessing nutrition-related clinical outcomes among surgical critically ill patients.\n\nThe main questions it aims to answer are:\n\nDoes guideline implementation improve ICU healthcare professionals' adherence to recommended clinical nutrition practice guidelines?\n\nDoes the implementation of the clinical nutrition practice guideline improve the proportion of surgical critically ill patients who achieve recommended energy and protein intake targets during ICU stay?\n\nResearchers will compare outcomes before and after guideline implementation to determine whether the i-PARIHS-guided guideline translation improves nutrition management processes, healthcare professional performance, and patient-related clinical outcomes.\n\nParticipants will:\n\nComplete baseline and post-implementation assessments related to clinical nutrition knowledge, attitudes, and practices.\n\nParticipate in guideline-based education, training, and implementation activities guided by the i-PARIHS framework.\n\nApply the adapted clinical nutrition practice guideline during routine clinical care in surgical ICUs.\n\nBe evaluated through on-site audits, questionnaires, and clinical data collection during the implementation process.",[26,27,28,29,30],"ICU Patients","Surgical","Nutrition Intervention","Enteral Nutrition","Enteral Nutrition Intolerance",[32,33,34,35,36],"Clinical Nutrition","Surgical Intensive Care Units","i-PARIHS Framework","Implementation Science","Clinical practice guideline","NOT_YET_RECRUITING","2026-01-11",{"date":40,"type":41},"2026-01-13","ACTUAL",{"date":43,"type":20},"2025-12-20",{"date":45,"type":20},"2026-12-31",{"name":47,"class":48},"Xuanwu Hospital, Beijing","OTHER",{"id":50,"slug":51,"hasResults":11,"nctId":52,"briefTitle":53,"officialTitle":53,"acronym":54,"eligibilityCriteria":55,"healthyVolunteers":11,"sex":56,"minAge":17,"maxAge":4,"enrollmentInfo":57,"targetDuration":59,"studyType":60,"phases":4,"briefSummary":61,"conditions":62,"keywords":66,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":75,"completionDateStruct":77,"leadSponsor":79,"locationsCount":81},"100543512","national-registry-of-surgical-treatment-and-percutaneous-cryoablation-of-parietal-endometriosis-100543512","NCT06356831","National Registry of Surgical Treatment and Percutaneous Cryoablation of Parietal Endometriosis","Endomercyo","Inclusion Criteria:\n\n* Presence of parietal endometriosis: with suggestive clinical and imaging criteria (MRI and ultrasound)\n* Symptomatic parietal endometriosis (VAS \\> 3 OR bothersome bleeding OR reported impact on quality of life)\n\nExclusion Criteria:\n\n* Endometriosis not affecting the anterior wall of the abdomen (as deep pelvic muscle: ilio-psoas, obturators, perineal, ischio-anal fossa)\n* Minor patient (\\\u003C 18 years)\n* Pregnant patient at any trimester\n* Patient with hemostasis disorders (constitutional or acquired)\n* Patient with systemic infection or localized scar infection upon inclusion.\n* Patient with contraindications to MRI\n* Female patient with a planned medical or surgical procedure for the duration of the study that may interfere with the proper conduct of the study.\n* Patient unable to understand the information provided\n* Patient who is not affiliated to the social security system\n* Patient under curatorship or tutorship\n* Patient with a nodule of primary or secondary malignant tumor origin","FEMALE",{"count":58,"type":20},300,"3 Years","OBSERVATIONAL","National multicentric registry of a cohort of patient with suffering parietal endometriosis, carried out by a multidisciplinary radiosurgery team",[63,64,27,65],"Endometriosis","Cryotherapy Effect","Radiology",[67,68,69,70],"endometriosis","Cryo ablation","Surgical operation","radiology","RECRUITING","2025-11-26",{"date":74,"type":41},"2025-11-28",{"date":76,"type":41},"2024-06-15",{"date":78,"type":20},"2028-01-31",{"name":80,"class":48},"Centre Hospitalier Intercommunal Creteil",18,{"id":83,"slug":84,"hasResults":11,"nctId":85,"briefTitle":86,"officialTitle":87,"acronym":4,"eligibilityCriteria":88,"healthyVolunteers":11,"sex":56,"minAge":17,"maxAge":89,"enrollmentInfo":90,"targetDuration":4,"studyType":21,"phases":92,"briefSummary":93,"conditions":94,"keywords":4,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":100,"lastUpdatePostDateStruct":101,"startDateStruct":103,"completionDateStruct":104,"leadSponsor":106,"locationsCount":108},"100580456","ultrasound-guided-versus-surgical-rectus-sheath-block-versus-local-anesthesia-infiltration-for-postoperative-analgesia-in-patients-undergoing-total-abdominal-hysterectomy-100580456","NCT06837532","Ultrasound Guided Versus Surgical Rectus Sheath Block Versus Local Anesthesia Infiltration for Postoperative Analgesia in Patients Undergoing Total Abdominal Hysterectomy","Ultrasound Guided Versus Surgical Rectus Sheath Block Versus Local Anesthesia Infiltration for Postoperative Analgesia in Patients Undergoing Total Abdominal Hysterectomy: A Randomized Trial","Inclusion Criteria:\n\n* Age from 18 to 65 years old.\n* American Society of Anesthesiologists (ASA) physical status I - II.\n* Patients scheduled for elective total abdominal hysterectomy under general anesthesia.\n\nExclusion Criteria:\n\n* Hepatic, renal or cardiac disease.\n* Any known allergy to local anesthetic.\n* Physical or mental conditions which may vaguely measure postoperative pain following surgery.\n* History of chronic use of analgesic as nonsteroidal anti-inflammatory drugs (NSAIDs) or central nervous system (CNS) depressants as antiepileptic, and bleeding disorders.","65 Years",{"count":91,"type":20},90,[23],"The aim of this work is to compare the efficacy and safety of the effectiveness and safety of ultrasound-guided surgical rectus sheath block and local anesthetic infiltration for postoperative analgesia in patients undergoing total abdominal hysterectomy.",[95,27,96,97,98,99],"Ultrasound","Rectus Sheath Block","Local Anesthesia Infiltration","Postoperative Analgesia","Total Abdominal Hysterectomy","2025-02-20",{"date":102,"type":41},"2025-02-21",{"date":100,"type":41},{"date":105,"type":20},"2025-08-01",{"name":107,"class":48},"Ain Shams University",1]