[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"point-of-care-ultrasound-pocus\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:point-of-care-ultrasound-pocus":31},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,10,0,[8,56,85,112,135,164,202,227,259,284],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":37,"overallStatus":43,"whyStopped":4,"lastUpdateSubmitDate":44,"lastUpdatePostDateStruct":45,"startDateStruct":48,"completionDateStruct":50,"leadSponsor":52,"locationsCount":55},"100605188","cardiac-point-of-care-ultrasound-training-pathway-for-emergency-department-advanced-practice-providers-100605188",false,"NCT07159269","Cardiac point-of Care Ultrasound Training Pathway for Emergency Department Advanced Practice Providers","Cardiac Point-of-care Ultrasound Clinical Training Pathway Implementation and Impact Assessment for Advanced Practice Providers in the Emergency Department","Inclusion Criteria:\n\n* advanced practice providers (APPs) currently working in our ED, with additional APPs as they are hired (expected to be about 75 APPs total within the next 3 years due to expanding staffing needs and coverage models).\n\nExclusion Criteria:\n\n* non-APPs such as physicians, nurses, or other clinical staff",true,"ALL","18 Years",{"count":20,"type":21},75,"ESTIMATED","INTERVENTIONAL",[24],"NA","The aim of this study is to assess emergency medicine physician and advanced practice provider (APP) knowledge and technical skill in performance of a point-of-care ultrasound simulation and just-in-time training pathway to determine the feasibility, acceptability, and usability of the ultrasound training program. By performing this study, we hope to create a standardized training model which could potentially facilitate point-of-care ultrasound (POCUS) clinical performance and thereby improve patient care.",[27,28,29,30,31,32,33,34,35,36],"Cardiovascular Disease Acute","Emergency Department Patient","Heart Failure Acute","Pulmonary Embolism (Diagnosis)","Point of Care Ultrasound (POCUS)","Cardiac Tamponade","Pericardial Effusion","Diagnostic Imaging","Medical Training","Implementation Science",[38,39,40,41,42],"point of care ultrasound","focused cardiac ultrasound","advanced practice provider training","medical education","implementation science","RECRUITING","2026-06-01",{"date":46,"type":47},"2026-06-03","ACTUAL",{"date":49,"type":47},"2025-11-13",{"date":51,"type":21},"2030-06-30",{"name":53,"class":54},"Duke University","OTHER",1,{"id":57,"slug":58,"hasResults":11,"nctId":59,"briefTitle":60,"officialTitle":61,"acronym":62,"eligibilityCriteria":63,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":64,"targetDuration":4,"studyType":22,"phases":65,"briefSummary":66,"conditions":67,"keywords":71,"overallStatus":43,"whyStopped":4,"lastUpdateSubmitDate":76,"lastUpdatePostDateStruct":77,"startDateStruct":79,"completionDateStruct":81,"leadSponsor":83,"locationsCount":55},"100615381","central-venous-catheter-placement-with-thoracic-ultrasound-and-intracavity-ecg-positioning-100615381","NCT07291869","Central Venous Catheter Placement With Thoracic Ultrasound and Intracavity ECG Positioning","A Randomised Feasibility Study of Real-time Intracavity ECG and Thoracic Ultrasound for Central Venous Catheter Tip Confirmation in Critical Care","CVC-TIP","Inclusion Criteria:\n\n* Adult (aged ≥ 18 years)\n* Admitted, or planned for admission, to critical care\n* Requiring central venous catheter insertion as a part of their usual care\n* Suitable for both right or left internal jugular vein insertion\n\nExclusion Criteria:\n\n* Previously randomised into CVC-TIP\n* Atrial fibrillation on 12-lead ECG\n* Cardiovascular instability, defined as\n* Noradrenaline dose \\> 0.5mcg\u002Fkg\u002Fmin\n* Rapidly escalating doses of vasopressors \u002F inotropes\n* Difficulty in obtaining thoracic ultrasound images due to either\n* Weight \\> 120kg\n* Existing pneumothorax (either side)\n* Subcutaneous emphysema\n* Wounds \u002F dressing over anterior chest wall\n* Existing pacemaker\n* Non-English speaking participants\n* Death perceived as imminent\n* Any other reason as determined by treating clinician",{"count":20,"type":21},[24],"The goal of this interventional study is to assess the feasibility of two bedside techniques for confirming central venous catheter (CVC) placement and detecting complications:\n\n* Intracavity ECG monitoring to confirm internal jugular vein CVC tip position.\n* Thoracic point-of-care ultrasound (POCUS) to rule out pneumothorax following CVC insertion.\n\nParticipants who require an internal jugular CVC as part of their routine care and meet all inclusion and no exclusion criteria will be randomised to receive either:\n\n* Standard care, or\n* The intervention, consisting of intracavity ECG guidance and thoracic POCUS. The CVC will be inserted either on the left or right side of the neck.\n\nAll participants will undergo a post-procedure chest X-ray regardless of study arm, to allow comparison of the intervention methods with standard care.",[68,31,69,70],"Central Venous Catheter","Intracavitary Electrocardiogram Guiding","Feasibility Studies",[72,73,74,75],"Intracavity ECG","POCUS","IC-ECG","Thoracic point of care ultrasound","2026-05-28",{"date":78,"type":47},"2026-06-02",{"date":80,"type":47},"2026-05-15",{"date":82,"type":21},"2027-10",{"name":84,"class":54},"York Teaching Hospitals NHS Foundation Trust",{"id":86,"slug":87,"hasResults":11,"nctId":88,"briefTitle":89,"officialTitle":90,"acronym":4,"eligibilityCriteria":91,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":92,"targetDuration":4,"studyType":94,"phases":4,"briefSummary":95,"conditions":96,"keywords":99,"overallStatus":43,"whyStopped":4,"lastUpdateSubmitDate":103,"lastUpdatePostDateStruct":104,"startDateStruct":106,"completionDateStruct":108,"leadSponsor":110,"locationsCount":55},"100638301","assessment-of-lvot-vti-in-healthy-volunteers-100638301","NCT07600931","Assessment of LVOT VTI in Healthy Volunteers","Reproducibility, Intra- and Inter-Observer Variability of Bedside Cardiac Ultrasound Measurements in the Assessment of Hemodynamic Parameters in Healthy Volunteers","Inclusion Criteria:\n\n* Age \\> 18 years,\n* Medical student at Medical University of Warsaw or licensed physician.\n\nExclusion Criteria:\n\n* Age \\\u003C 18 years,\n* Prior experience in performing cardiac ultrasound examinations, including acquisition of apical five- and three-chamber views and Doppler measurements of LVOT VTI.",{"count":93,"type":21},30,"OBSERVATIONAL","Healthy subjects will have transthoracic echocardiography evaluation of Left Ventricular Outflow Tract Velocity-Time Integral (LVOT VTI) performed by operators after brief training.",[97,98,31],"Hemodynamic Assessment","Bedside Ultrasonography",[97,100,98,101,102],"Velocity-Time Integral","Point of care ultrasound","Critical care","2026-05-14",{"date":105,"type":47},"2026-05-22",{"date":107,"type":21},"2026-05-11",{"date":109,"type":21},"2027-01",{"name":111,"class":54},"Medical University of Warsaw",{"id":113,"slug":114,"hasResults":11,"nctId":115,"briefTitle":116,"officialTitle":117,"acronym":4,"eligibilityCriteria":118,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":119,"targetDuration":4,"studyType":22,"phases":121,"briefSummary":122,"conditions":123,"keywords":124,"overallStatus":43,"whyStopped":4,"lastUpdateSubmitDate":126,"lastUpdatePostDateStruct":127,"startDateStruct":129,"completionDateStruct":131,"leadSponsor":133,"locationsCount":55},"100635719","point-of-care-ultrasound-utility-in-the-free-clinic-setting-100635719","NCT07556341","Point-of-care Ultrasound Utility in the Free Clinic Setting","Point-of-care Ultrasound Utility in the Free Clinic Setting: A Single Site Observational Study of Point of Care Ultrasound Utilization in a Free Clinic of Indianapolis, Indiana","Inclusion Criteria:\n\n* Patients \\>18 years old\n* Presenting to either: street medicine team in Indianapolis, IN OR patients presenting to free clinic in Indianapolis, IN, AND Being treated by the Primary Investigatory AND Meeting one or more of specific indications (see study design)\n\nExclusion Criteria:\n\n* Patients \\\u003C18 years old\n* Patients unable to provide verbal consent\n* Patient refusal of ultrasound",{"count":120,"type":21},50,[24],"The goal of this observational study is to learn about the clinical utility of point-of-care ultrasound (POCUS) in patients receiving care in a free clinic or street medicine setting in Indianapolis. The main question it aims to answer is:\n\nHow often is POCUS used during patient encounters in a free clinic setting, and how does it influence clinical decision-making?\n\nParticipants who are receiving care from the street medicine team or the Indiana University School of Medicine Student Outreach Clinic and who undergo a clinically indicated POCUS exam as part of their regular medical care will have information from their ultrasound encounters recorded. Researchers will track the type of ultrasound performed, the findings, and whether the ultrasound changed the patient's medical management. Participants will also have a 30-day follow-up through electronic medical record review or phone\u002Femail contact to assess their clinical course and compare POCUS findings with any formal radiology studies if performed.",[31],[38,125],"free clinic","2026-04-22",{"date":128,"type":47},"2026-04-29",{"date":130,"type":21},"2026-04",{"date":132,"type":21},"2026-07",{"name":134,"class":54},"Indiana University",{"id":136,"slug":137,"hasResults":11,"nctId":138,"briefTitle":139,"officialTitle":140,"acronym":141,"eligibilityCriteria":142,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":143,"targetDuration":4,"studyType":22,"phases":145,"briefSummary":146,"conditions":147,"keywords":150,"overallStatus":43,"whyStopped":4,"lastUpdateSubmitDate":154,"lastUpdatePostDateStruct":155,"startDateStruct":157,"completionDateStruct":159,"leadSponsor":161,"locationsCount":163},"100635222","the-spotlight-study-early-identification-of-post-surgical-infections-using-bedside-ultrasound-100635222","NCT07549880","The Spotlight Study: Early Identification of Post-Surgical Infections Using Bedside Ultrasound.","Post-Laparotomy Fluid Monitoring With Point of Care Ultrasonography : Predicting Surgical Site Infection & Optimizing Patient Convalescence (SPOTLIGHT Study).","SPOTLIGHT","Inclusion Criteria:\n\n* Adults \\>18 years.\n* Undergoing emergency or elective laparotomy.\n* Primary or delayed primary wound closure (DPC).\n* Wound classification: clean, clean-contaminated, contaminated, or dirty.\n* Informed consent obtained.\n\nExclusion Criteria:\n\n* Laparoscopic surgery\n* Wounds healing by secondary intention.\n* Ongoing wound dehiscence treatment with Negative Pressure Wound Therapy (NPWT).\n* Non-Danish residents",{"count":144,"type":21},100,[24],"Introduction:\n\nThe goal of this observational study is to learn whether point-of-care ultrasound (POCUS) can help detect early fluid build-up under the skin after open abdominal surgery (laparotomy) and whether these findings can predict surgical site infection. The study includes adults who recently had emergency or planned open abdominal surgery.\n\nHypothesis:\n\nThe main questions it aims to answer are:\n\n1. Does ultrasound identify subcutaneous fluid collections early after surgery?\n2. Do these fluid collections help predict which participants will develop a surgical site infection?\n\nIntervention:\n\nParticipants will:\n\n1. Have a superficial wound swab taken once at the start of the study (for research only).\n2. Receive three ultrasound scans of their surgical wound during days 1-3, 4-6, and 7-9 after surgery.\n3. Have their wound checked for redness, swelling, tenderness, or discharge before each scan.\n4. Be followed for 7 and 30 days after surgery (and up to 90 days if they have implanted mesh) to see whether an infection develops.\n\nUltrasound is non-invasive and safe. According to the protocol, \"no serious adverse effects are expected,\" though some participants may feel brief discomfort from pressure on a tender wound.\n\nThis study will help researchers understand whether routine bedside ultrasound can support earlier detection of wound infections and improve postoperative care in the future.",[148,149,31],"Surgical Site Infection (SSI)","Emergency Laparotomies",[151,152,153],"point of care ultrasound (POCUS)","surgical site infection (SSI)","Emergency laparotomies","2026-04-17",{"date":156,"type":47},"2026-04-24",{"date":158,"type":47},"2026-04-10",{"date":160,"type":21},"2027-08-30",{"name":162,"class":54},"Slagelse Hospital",3,{"id":165,"slug":166,"hasResults":11,"nctId":167,"briefTitle":168,"officialTitle":169,"acronym":170,"eligibilityCriteria":171,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":172,"targetDuration":4,"studyType":22,"phases":174,"briefSummary":177,"conditions":178,"keywords":185,"overallStatus":192,"whyStopped":4,"lastUpdateSubmitDate":193,"lastUpdatePostDateStruct":194,"startDateStruct":196,"completionDateStruct":198,"leadSponsor":200,"locationsCount":55},"100629059","phase-2-pocus-intervention-for-tailoring-diuretic-strategy-in-acute-decompensated-heart-failure-100629059","NCT07469722","POcus INTERvention for Tailoring Diuretic Strategy in Acute Decompensated Heart Failure","Point-of-care Ultrasound Intervention for Tailoring Diuretic Strategy in Acute Decompensated Heart Failure","POINTER-HF","Inclusion Criteria:\n\n* Men or women aged 18 years or older.\n* Diagnosis of acute decompensated heart failure (ADHF) with left ventricular ejection fraction \\\u003C50%, presenting with symptoms (dyspnea, orthopnea, fatigue) and\u002For signs (pulmonary crackles, peripheral edema, jugular venous distension, hepatomegaly, hepatojugular reflux) of decompensated heart failure.\n* Brain natriuretic peptide (BNP) ≥ 300 pg\u002FmL.\n* Signs of systemic and\u002For pulmonary congestion on POCUS, defined as DUCS ≥ 3 points.\n* Time from hospital admission ≤ 48 hours.\n* Signed informed consent.\n\nExclusion Criteria:\n\n* Patients under evaluation for heart transplantation or with prior heart transplantation.\n* Acute coronary syndrome as the primary cause of hospitalization.\n* Evidence of uncontrolled infection.\n* Cardiac surgery or percutaneous coronary or structural cardiac intervention within the previous 30 days.\n* Signs of hypoperfusion, defined as any of the following: mean arterial pressure \\\u003C 60 mmHg, capillary refill time \\> 4 seconds, arterial lactate \\> 2 mmol\u002FL or venous lactate \\> 2.5 mmol\u002FL.\n* Acute pulmonary embolism (segmental or more proximal) as the primary cause of hospitalization.\n* Acute stroke.\n* Chronic kidney disease stage 5 (estimated glomerular filtration rate \\\u003C 15 ml\u002Fmin\u002Fm²) or requirement for renal replacement therapy.\n* Liver cirrhosis with portal hypertension.\n* Known pulmonary disease with extensive parenchymal involvement, including interstitial lung disease, pulmonary metastases, prior pneumonectomy, lobectomy, or pleurodesis.\n* Severe hypokalemia (serum potassium \\\u003C 2.5 mmol\u002FL).\n* Pregnancy or breastfeeding.\n* Refusal to participate in the clinical trial.",{"count":173,"type":21},128,[175,176],"PHASE2","PHASE3","Acute decompensated heart failure (ADHF) is a frequent cause of hospitalization and is associated with high morbidity and mortality. Congestion is the primary pathophysiological mechanism leading to clinical deterioration and hospitalization in ADHF. Diuretics remain the cornerstone of treatment for most ADHF phenotypes; however, evidence regarding optimal strategies to guide diuretic therapy during the decongestion process is limited. Recently, point-of-care ultrasound (POCUS) has emerged as a promising tool to support clinical assessment in ADHF, improving diagnostic accuracy, prognostication, and pre-discharge evaluation. Nevertheless, the role of POCUS in guiding therapeutic management in ADHF remains uncertain. To specifically assess congestion in patients with ADHF, a pragmatic POCUS-based score, the Dynamic Ultrasound Congestion Score (DUCS), was developed. DUCS integrates lung ultrasound and Venous Excess Ultrasound (VExUS) to dynamically evaluate congestion severity, treatment response, and therapeutic goals during ADHF management. Observational data suggest that DUCS is associated with in-hospital outcomes and short-term prognosis, and correlates with markers of decongestion such as urinary output and weight loss. This study is a randomized, single-center, single-blind clinical trial designed to evaluate whether a DUCS-guided POCUS strategy improves clinical and decongestion outcomes compared with standard of care. Eligible patients hospitalized due to ADHF will be randomized within 48 hours of admission to one of two groups: (1) diuretic treatment guided by institutional standard-of-care combined with information from the EVEREST congestion score assessment and guideline-based treatment recommendations; or (2) diuretic treatment guided by serial DUCS-based POCUS assessments used to inform diuretic adjustment recommendations. Participants in both groups will undergo evaluations at baseline (day 1), day 2, day 3 and day 5, including clinical data collection, physical examination using the EVEREST congestion score, and standardized DUCS-based POCUS assessments. Outcomes to be assessed include in-hospital mortality, length of hospital stay, decongestion parameters, and changes in biomarkers.",[179,180,181,182,183,184],"Acute Heart Failure (AHF)","Congestive Heart Failure Acute","Diuretic Effect","Lung Ultrasonography Score","Ultrasonography, Doppler","Point-of-care Ultrasound (POCUS)",[186,187,188,189,190,191],"Acute Heart Failure","Congestive Heart Failure","Point-of-Care Ultrasound","Lung Ultrasound","Venous Excess Ultrasound","Diuretic","NOT_YET_RECRUITING","2026-03-16",{"date":195,"type":47},"2026-03-18",{"date":197,"type":21},"2026-03-23",{"date":199,"type":21},"2028-07-01",{"name":201,"class":54},"Hospital de Clinicas de Porto Alegre",{"id":203,"slug":204,"hasResults":11,"nctId":205,"briefTitle":206,"officialTitle":206,"acronym":207,"eligibilityCriteria":208,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":209,"targetDuration":4,"studyType":94,"phases":4,"briefSummary":210,"conditions":211,"keywords":214,"overallStatus":43,"whyStopped":4,"lastUpdateSubmitDate":218,"lastUpdatePostDateStruct":219,"startDateStruct":221,"completionDateStruct":223,"leadSponsor":225,"locationsCount":55},"100626667","internal-jugular-vein-ultrasound-for-volume-status-assessment-in-haemodialysis-100626667","NCT07438613","Internal Jugular Vein Ultrasound for Volume Status Assessment in Haemodialysis","IJV-US","Inclusion Criteria:\n\n* Chronic haemodialysis\n* Informed consent\n\nExclusion Criteria:\n\n* Non ultrafiltrative treatment\n* Insufficient compliance",{"count":144,"type":21},"To Evaluate accuracy of Internal Jugular Vein Point-of-Care ultrasound for volume status evaluation in chronic haemodialysis",[212,213,31],"Haemodialysis","Volume Assessment",[215,216,217],"haemodialysis","volume assessment","PoCUS","2026-02-22",{"date":220,"type":47},"2026-02-27",{"date":222,"type":47},"2025-09-15",{"date":224,"type":21},"2027-09",{"name":226,"class":54},"University of Bologna",{"id":228,"slug":229,"hasResults":11,"nctId":230,"briefTitle":231,"officialTitle":231,"acronym":4,"eligibilityCriteria":232,"healthyVolunteers":16,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":233,"targetDuration":4,"studyType":94,"phases":4,"briefSummary":235,"conditions":236,"keywords":239,"overallStatus":192,"whyStopped":4,"lastUpdateSubmitDate":249,"lastUpdatePostDateStruct":250,"startDateStruct":252,"completionDateStruct":254,"leadSponsor":256,"locationsCount":258},"100621548","evaluation-of-an-online-application-for-point-of-care-ultrasound-training-in-general-internal-medicine-residents-100621548","NCT07372053","Evaluation of an Online Application for Point of Care Ultrasound Training in General Internal Medicine Residents","Inclusion Criteria:\n\n* General Internal Medicine resident employed at one of the study sites for at least 2 months\n* Probably or definitely interested in achieving POCUS certification (mandatory for the General Internal Medicine specialisation in Switzerland)\n* Basic ultrasound course completed (Basic course Abdominal ultrasound or Emergency ultrasound)\n* Will spend at least 3 months within a rotation where POCUS training is offered during the 6 months after baseline assessment\n\nExclusion Criteria:\n\n* Definitely or probably not interested in achieving POCUS certification\n* Has already performed more than 80 supervised and more than 160 total POCUS exams\n* Will end employment at the study site less than 7 months after baseline assessment",{"count":234,"type":21},56,"This study compares Point of Care Ultrasound (POCUS) training in two hospitals, one that uses an online application for supervision and one that does not use the application. The goal of this trial is to learn if POCUS supervision using the online application is associated with improved POCUS skills in residents in General Internal Medicine (GIM). The main question it aims to answer is:\n\n\\- Do POCUS skills improve more during 6 months in GIM residents supervised using the application than in GIM residents who do not use the application?\n\nFurther questions the study aims to answer are:\n\n* Do residents using the application perform more POCUS exams during 6 months than residents not using the application?\n* Are residents using the application more satisfied with their POCUS training than residents not using the application?",[31,237,238],"Ultrasound Exam in Emergency\u002FMedical Care","Ultrasound Evaluation",[73,240,241,242,243,244,245,246,247,248],"Point of Care Ultrasound","Point of Care Ultrasonography","Medical Education","Ultrasound Education","POCUS Training","POCUS Education","Ultrasound Supervision","POCUS Supervision","Ultrasound Training","2026-01-20",{"date":251,"type":47},"2026-01-28",{"date":253,"type":21},"2026-02",{"date":255,"type":21},"2028-01",{"name":257,"class":54},"Kantonsspital Baden",2,{"id":260,"slug":261,"hasResults":11,"nctId":262,"briefTitle":263,"officialTitle":263,"acronym":264,"eligibilityCriteria":265,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":266,"targetDuration":268,"studyType":94,"phases":4,"briefSummary":269,"conditions":270,"keywords":4,"overallStatus":192,"whyStopped":4,"lastUpdateSubmitDate":275,"lastUpdatePostDateStruct":276,"startDateStruct":278,"completionDateStruct":280,"leadSponsor":282,"locationsCount":55},"100570462","italian-data-registry-of-patients-undergoing-peripheral-nerve-block-performed-in-the-emergency-departments-100570462","NCT06707558","Italian Data Registry of Patients Undergoing Peripheral Nerve Block Performed in the Emergency Departments","ED-RA","Inclusion Criteria:\n\n* Age ≥18 years;\n* NRS\\>3\n* Patients with traumatic fractures of ≤2 districts (radiologically confirmed (RX or CT). Districts are:\n\nChest (one hemilateral) Pelvis (one hemilateral) Femur Leg Ankle Foot Shoulder Humerus Forearm Hand\u002Ffingers\n\n\\- Presence of written informed consent to the study.\n\nExclusion Criteria:\n\n* Intubated patients\n* Patients with known dementia\n* Patients with delirium (assessed by Confusion Assessment Method)\n* Pregnant patients\n* Patients with allergies to local anesthetics\n* Patients unable to adequately communicate pain",{"count":267,"type":21},500,"7 Days","This data registry aim is to describe the practice of Point-of-Care Ultrasound Guided Regional Anaesthesia (POCUS-GRA) in emergency departments of nosocomial hospitals where, the organizational structure, has already provided for the implementation of peripheral nerve blocks (PNB) in common clinical practice for the treatment of acute pain due to bone fractures.",[271,31,272,273,274],"Emergency","Anesthesia","Acute Pain","Trauma","2024-11-26",{"date":277,"type":47},"2024-11-29",{"date":279,"type":21},"2024-12-10",{"date":281,"type":21},"2025-12-31",{"name":283,"class":54},"Azienda Ospedaliera SS. Antonio e Biagio e Cesare Arrigo di Alessandria",{"id":285,"slug":286,"hasResults":11,"nctId":287,"briefTitle":288,"officialTitle":289,"acronym":4,"eligibilityCriteria":290,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":291,"targetDuration":4,"studyType":94,"phases":4,"briefSummary":293,"conditions":294,"keywords":300,"overallStatus":43,"whyStopped":4,"lastUpdateSubmitDate":305,"lastUpdatePostDateStruct":306,"startDateStruct":308,"completionDateStruct":310,"leadSponsor":312,"locationsCount":55},"100565526","gastric-emptying-time-in-traumatic-injuries-100565526","NCT06643325","Gastric Emptying Time in Traumatic Injuries","Gastric Point-of-care Sonography with Focus on Gastric Emptying Time in Patients with Traumatic Injuries. a Prospective Observational Study","Inclusion Criteria:\n\n* relevant traumatic injury\n\nExclusion Criteria:\n\n* life-threatening traumatic injury (immediate treatment is necessary)\n* Underage\n* Known pregnancy",{"count":292,"type":21},200,"The investigators plan to do serial sonographic examinations of the gastric antrum (quantity, quality) to estimate the gastric emptying time and dependant factors after traumatic injurys.",[272,295,296,31,297,298,299],"Gastric Ultrasound","Sonography","Regurgitation","Pulmonary Aspiration During Anesthetic Induction","Trauma Patients",[38,301,302,303,304],"gastric ultrasound","trauma patients","aspiration","anesthesia","2024-10-14",{"date":307,"type":47},"2024-10-16",{"date":309,"type":47},"2023-02-01",{"date":311,"type":21},"2025-09-30",{"name":313,"class":54},"Kantonsspital Winterthur KSW"]