[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"trauma-patients\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:trauma-patients":30},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,7,0,[8,51,81,103,140,166,200],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":24,"conditions":25,"keywords":31,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":39,"lastUpdatePostDateStruct":40,"startDateStruct":43,"completionDateStruct":45,"leadSponsor":47,"locationsCount":50},"100608942","mortality-of-trauma-in-the-intensive-care-unit-100608942",false,"NCT07208110","Mortality of Trauma in the Intensive Care Unit.","Factors Associated With Mortality by Trauma in the Intensive Care Unit in Villavicencio, Colombia. A Trial Based on a Discharge Registry.","MOTRAM-ICU-COL","Inclusion Criteria:\n\n* Admitted to the intensive care unit.\n\nExclusion Criteria:\n\n* None.","ALL","15 Years","100 Years",{"count":21,"type":22},500,"ESTIMATED","OBSERVATIONAL","In this study, it was planned to establish the factors associated with severe trauma discharged from the intensive care unit and mortality. A cross-sectional trial will be conducted to review the ICU discharge database at a two-year interval to review records of trauma admissions patients and compare them with other types of admissions. Participant institutions are general hospitals (public and private) from the Colombian Orinoco region. the prevalence of admission by trauma will also be determined.",[26,27,28,29,30],"Trauma (Including Fractures)","Trauma ICU Patients","Trauma Injury","Trauma Patients in ICU","Trauma Patients",[32,33,34,35,36,37],"Trauma","Wounds and Injuries","Intensive Care Units","Trauma Registry","Low-Middle Income Countries","Colombia","RECRUITING","2026-05-25",{"date":41,"type":42},"2026-05-27","ACTUAL",{"date":44,"type":42},"2026-01-30",{"date":46,"type":22},"2028-12",{"name":48,"class":49},"Hospital Departamental de Villavicencio","OTHER",1,{"id":52,"slug":53,"hasResults":11,"nctId":54,"briefTitle":55,"officialTitle":55,"acronym":4,"eligibilityCriteria":56,"healthyVolunteers":57,"sex":17,"minAge":58,"maxAge":59,"enrollmentInfo":60,"targetDuration":4,"studyType":62,"phases":63,"briefSummary":65,"conditions":66,"keywords":4,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":75,"completionDateStruct":77,"leadSponsor":79,"locationsCount":4},"100638265","the-effect-of-aromatherapy-massage-based-sensory-stmulaton-program-on-cogntve-and-sensory-functon-n-intensve-care-patents-100638265","NCT07593430","The Effect of Aromatherapy Massage-Based Sensory Stımulatıon Program on Cognıtıve and Sensory Functıon ın Intensıve Care Patıents","Inclusion Criteria:\n\n* Patients diagnosed with acute brain injury,\n* Glasgow Coma Score (GCS) between 6 and 12,\n* Intubated or monitored on oxygen,\n* 18 years of age or older,\n* Between 24 and 48 hours after hemodynamic vital signs stabilized and without a history of delirium,\n* Patients without a history of diseases that increase the risk of odor sensitivity, such as epilepsy or asthma,\n\nExclusion Criteria:\n\n* Glasgow Coma Score (GCS) below 6,\n* Hemodynamic instability,\n* Continuously using neuromuscular blocking agents during the study,\n* Changes in treatment schedule during the study,\n* History of diseases that increase the risk of odor sensitivity, such as epilepsy or asthma,",true,"18 Years","90 Years",{"count":61,"type":22},60,"INTERVENTIONAL",[64],"NA","Background: Sensory stimulation is a treatment that uses auditory, visual, tactile, gustatory, and olfactory stimuli, as well as balance and position modes, with intensity and frequency adjusted to the patient's individual thresholds to increase the frequency of arousal, awareness, and pronounced behavioral responses. Studies have shown that sensory stimulation, especially when applied from the beginning of the patient's hospitalization, can shorten the average length of stay and reduce patient anxiety. Among the TIT methods applied by nurses, touch, music therapy, and aromatherapy are included as applications that can be applied to the sensory input problems of intensive care patients and can positively affect their sensory perceptions.Objective: This study is planned to be conducted as a randomized controlled single-blind study to determine the effect of a sensory stimulation program performed with aromatherapy massage applied twice daily for 7 days with a mixture of orange, patchouli, and rosemary oil (7 drops of sweet orange oil, 5 drops of patchouli oil, and 3 drops of rosemary oil in 50 ml of jojoba oil) on the cognitive sensory perception level of patients monitored on mechanical ventilation or oxygen in the ICU.Method: In the study, all patients hospitalized in the tertiary care ICU of the University's Training and Research Hospital will constitute the population. Randomized sampling method will be used in the study. Sample size; G\\*power 3.5.1. In the power analysis performed with the software package, it is planned that each group will consist of at least 20 people to determine an effect size of 1% with an alpha risk of 0.05 and a power of 0.80 in line with the literature. The data collection tools to be used are: Patient Identification Form, Patient Monitoring Form, Medication Monitoring Form, Glasgow Coma Scale, Rancho Los Amigos Cognitive Function Scale. In Intervention Group 1, massage will be performed by the lead researcher ICU nurse, and the sensory stimulation program will be performed by a trained family member. In Intervention Group 2, massage will be performed by the lead researcher ICU nurse, and the sensory stimulation program will be performed by a nurse. Routine care will be provided to the control group. Since the groups are compared, the independent samples t-test and the Shapiro-Wilk test, which are parametric tests, will be used for evaluation.",[67,68,69,70,30],"Cognitive Sensory Perception Level","in Unconscious Patients","Lung Disaases","Cerebro Vascular Disease","NOT_YET_RECRUITING","2026-05-13",{"date":74,"type":42},"2026-05-18",{"date":76,"type":22},"2026-06-01",{"date":78,"type":22},"2027-06",{"name":80,"class":49},"Nigde Omer Halisdemir University",{"id":82,"slug":83,"hasResults":11,"nctId":84,"briefTitle":85,"officialTitle":85,"acronym":4,"eligibilityCriteria":86,"healthyVolunteers":11,"sex":17,"minAge":58,"maxAge":87,"enrollmentInfo":88,"targetDuration":90,"studyType":23,"phases":4,"briefSummary":91,"conditions":92,"keywords":4,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":94,"lastUpdatePostDateStruct":95,"startDateStruct":97,"completionDateStruct":99,"leadSponsor":101,"locationsCount":4},"100633726","analysis-of-influencing-factors-for-the-development-of-ptsd-in-emergency-department-trauma-patients-100633726","NCT07530432","Analysis of Influencing Factors for the Development of PTSD in Emergency Department Trauma Patients","Inclusion Criteria:\n\n* Age between 18 and 65 years old (inclusive);\n* Experienced a life-threatening major traumatic event, clearly diagnosed by a clinician;\n* The patient is able to communicate normally with medical staff through language;\n* The subject is fully informed and voluntarily signs the informed consent form.\n\nExclusion Criteria:\n\n* History of psychiatric disorders or current use of psychotropic medications;\n* Pre-existing cognitive impairment (e.g., dementia, Alzheimer's disease);\n* Terminal illnesses (such as advanced malignant tumors, end-stage organ failure, advanced neurological diseases, or any other condition judged by the attending physician to have a life expectancy of less than 6 months);\n* Inability to cooperate with follow-up.","65 Years",{"count":89,"type":22},250,"6 Months","The goal of this observational study is to learn about the long-term effects of key factors such as cognitive flexibility, social support, and physiological stress on the occurrence of Post-Traumatic Stress Disorder (PTSD) in adult trauma patients treated in the emergency department. The main question it aims to answer is:\n\nAmong emergency department patients who have experienced major trauma, can factors such as early post-trauma cognitive flexibility, level of social support, inflammatory markers, and trauma severity predict the development of PTSD within 6 months? Participants will complete a series of online questionnaires and clinical assessments at baseline, 1 month, 3 months, and 6 months after the traumatic event.",[30,93],"PTSD","2026-04-08",{"date":96,"type":42},"2026-04-15",{"date":98,"type":22},"2026-03-20",{"date":100,"type":22},"2026-12",{"name":102,"class":49},"The First Affiliated Hospital of Air Force Medicial University",{"id":104,"slug":105,"hasResults":11,"nctId":106,"briefTitle":107,"officialTitle":108,"acronym":109,"eligibilityCriteria":110,"healthyVolunteers":11,"sex":17,"minAge":58,"maxAge":87,"enrollmentInfo":111,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":113,"conditions":114,"keywords":119,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":130,"lastUpdatePostDateStruct":131,"startDateStruct":133,"completionDateStruct":135,"leadSponsor":137,"locationsCount":50},"100630810","renal-and-hepatic-abnormal-doppler-patterns-in-trauma-100630810","NCT07492511","Renal and Hepatic Abnormal Doppler Patterns in Trauma","Renal and hEpatiC abnoRmal dopplEr pAtterns iN Trauma: a Multicentre Prospective Observational Study","RECREANT","Inclusion Criteria:\n\n* Age 18-65 years;\n* Admission within 24h from traumatic injury;\n* ISS \\>15\n\nExclusion Criteria:\n\n1. Age \\\u003C18 or \\>65;\n2. Known heart failure (NYHA ≥II);\n3. Chronic kidney disease (any stage) or chronic RRT;\n4. Chronic respiratory disease needing home O₂ or ventilation;\n5. Radiological evidence of vascular or parenchymal renal injury on trauma CT precluding reliable Doppler assessment",{"count":112,"type":22},350,"The goal of this observational study is to learn about renal and hepatic blood flow abnormalities detected by bedside ultrasound in adult patients admitted to the intensive care unit (ICU) following major trauma.\n\nThe main questions it aims to answer are:\n\n* How reliably can trained operators measure renal Doppler and venous congestion scores (RDRI and VExUS) across different hospitals?\n* How common are abnormal kidney and liver blood flow patterns in major trauma patients during the first 72 hours of ICU admission?\n* Are these abnormal patterns associated with acute kidney injury or the need for mechanical ventilation?\n\nParticipants admitted to ICUs or high-dependency units (HDUs) with major trauma (Injury Severity Score \\>15) will undergo non-invasive bedside ultrasound assessments at admission and at 24, 48, and 72 hours. No additional treatments or interventions will be given as part of this study. Kidney function will also be checked at 6 months after hospital discharge.",[26,30,115,116,117,118],"Kidney Disease","Hypovolemia","Hypervolemia","Kidney Failure",[120,121,122,123,124,125,126,127,128,129],"VEXUS","trauma","kidney injury","kidney failure","Venous congestion","renal perfusion","Renal Doppler resistive index","major trauma","Hemodynamic phenotyping","ICU","2026-03-19",{"date":132,"type":42},"2026-03-25",{"date":134,"type":42},"2026-03-01",{"date":136,"type":22},"2030-06-30",{"name":138,"class":139},"Azienda Usl di Bologna","OTHER_GOV",{"id":141,"slug":142,"hasResults":11,"nctId":143,"briefTitle":144,"officialTitle":145,"acronym":146,"eligibilityCriteria":147,"healthyVolunteers":11,"sex":17,"minAge":148,"maxAge":4,"enrollmentInfo":149,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":151,"conditions":152,"keywords":153,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":157,"lastUpdatePostDateStruct":158,"startDateStruct":160,"completionDateStruct":162,"leadSponsor":164,"locationsCount":50},"100607301","comparison-of-emtras-rems-and-gap-scores-in-trauma-100607301","NCT07186777","Comparison of EMTRAS, REMS, and GAP Scores in Trauma","Comparative Predictive Accuracy of EMTRAS, REMS, and GAP Scores for Mortality, Endotracheal Intubation, and Length of Hospitalization in Trauma Patients: The First Prospective Cohort Study From Iraq","TRAPS","Inclusion Criteria:\n\n* Patients presenting to the emergency department with trauma.\n* Patients or their legal guardians must provide informed consent to participate in the study.\n* Admission within 12 hours of injury.\n\nExclusion Criteria:\n\n* Patients with incomplete clinical data or those discharged before scoring can be performed.\n* Pregnant patients (due to specific physiological considerations not accounted for by the scoring system).\n* Patients who died before arrival or were declared dead on arrival.\n* Patients who refuse participation or for whom informed consent cannot be obtained.","16 Years",{"count":150,"type":22},188,"The goal of this prospective multicenter cohort study is to evaluate and compare the predictive utility of the EMTRAS, REMS, and GAP scores in determining key outcomes among trauma patients admitted to participating hospitals in Iraq. The primary outcomes of interest include mortality, the need for endotracheal intubation, and length of hospitalization.\n\nThe main questions it aims to answer are:\n\nHow accurately do EMTRAS, REMS, and GAP scores predict mortality in trauma patients?\n\nHow effective are these scores in predicting the need for endotracheal intubation?\n\nHow well do these scores correlate with hospitalization duration in trauma patients?\n\nParticipants will:\n\nBe assessed using EMTRAS, REMS, and GAP scores upon admission to the emergency department.\n\nHave their clinical outcomes, including survival, intubation requirements, and length of hospital stay, monitored throughout their hospitalization.",[30],[154,155,156,32],"EMTRAS","REMS","GAP","2026-03-03",{"date":159,"type":42},"2026-03-04",{"date":161,"type":42},"2025-09-15",{"date":163,"type":22},"2026-12-15",{"name":165,"class":49},"Al-Nahrain University",{"id":167,"slug":168,"hasResults":11,"nctId":169,"briefTitle":170,"officialTitle":171,"acronym":172,"eligibilityCriteria":173,"healthyVolunteers":11,"sex":17,"minAge":148,"maxAge":4,"enrollmentInfo":174,"targetDuration":4,"studyType":62,"phases":176,"briefSummary":177,"conditions":178,"keywords":185,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":191,"lastUpdatePostDateStruct":192,"startDateStruct":194,"completionDateStruct":196,"leadSponsor":198,"locationsCount":50},"100613601","assess-the-efficacy-of-tailored-patient-information-and-voluntary-patient-managed-outpatient-digital-follow-up-i-pod-as-an-adjunct-to-standard-treatment-according-to-national-guidelines-in-the-national-trauma-plan-among-adult-trauma-patients-in-norway-100613601","NCT07268716","Assess the Efficacy of Tailored Patient Information and Voluntary Patient-managed Outpatient Digital Follow-up (I-POD) as an Adjunct to Standard Treatment According to National Guidelines in the National Trauma Plan Among Adult Trauma Patients in Norway.","A Randomized Controlled Clinical Trial to Assess the Efficacy of Tailored Patient Information and Voluntary Patient-Managed Outpatient Digital Follow-Up as an Adjunct to Standard Treatment According to National Guidelines in Adult Trauma Patients in Norway (The POSTRAUMA Trial).","POSTRAUMA","Inclusion Criteria:\n\n* 16 years or older\n* Fulfils the national criteria for TTA and admitted to HUS following trauma\n* Included in NTR database\n* Able to give informed consent\n\nExclusion Criteria:\n\n* 15 years or younger\n* Not included in NTR database\n* Deceased before discharge from the hospital.\n* Not able to give informed consent\n* Insufficient command of the Norwegian language\n* Foreign tourists or nationals\n* Suicide attempt or serious self-inflicted trauma\n* Serious psychiatric disorders or serious ongoing substance abuse",{"count":175,"type":22},256,[64],"The POSTRAUMA trial is a clinical trial at The Regional trauma centre of Western Norway, Haukeland University Hospital.\n\nTrauma is the leading cause of death worldwide in patients aged 1-45 years. In Norway, approximately 10,000 patients are admitted to hospital annually due to trauma, with 66% being male. The mean age is 43 years for male and 48 years for female, indicating a relatively young patient population.\n\nWhile mortality rates are decreasing, a significant proportion of trauma survivors experience long-term disabilities, reduced quality of life, and difficulties in returning to work. These consequences impose substantial burdens on individuals, families, and society. Considering these issues, a shift in focus is needed-from survival alone to long-term functional recovery and quality of life after trauma.\n\nSevere trauma often requires long-term follow-up, both physically and psychosocially. Traditional follow-up can be fragmented and not tailored to individual needs. Digital patient monitoring and tailored information have the potential to improve patient pathways, but knowledge about how these are experienced by patients is limited.\n\nThe goal is to find out if Norwegian trauma patients who receive tailored patient information and patient-managed outpatient digital follow-up, in addition to standard treatment have:\n\n* Less disability\n* Return more often to work\n* Improved quality of life\n\nThe study population are Norwegian trauma patients, 16 years or older at date of inclusion, who are admitted to Haukeland University hospital (HUS) following trauma with trauma team activation. 256 patients will be included in this trial.\n\nParticipants will:\n\n* Answer a questionnaire at inclusion, one month, 6 months and 12 months.\n* Participants in the intervention group will be invited to digital outpatient follow up one month after the accident.\n* Some participants will be interviewed about how they experienced their trauma follow up.",[179,30,26,28,180,181,182,183,184],"Trauma Centers","Rehabilitation After Neurological or Orthopaedic Injuries","Rehabilitation","Return to Work","HRQOL (Health Related Quality Of Life)","EQ5D5L-VAS",[186,121,187,188,189,190],"multitrauma","rehabilitation","return to work","HRQOL","EQ5D","2025-12-16",{"date":193,"type":42},"2025-12-22",{"date":195,"type":22},"2026-03-02",{"date":197,"type":22},"2029-12-31",{"name":199,"class":49},"Haukeland University Hospital",{"id":201,"slug":202,"hasResults":11,"nctId":203,"briefTitle":204,"officialTitle":205,"acronym":4,"eligibilityCriteria":206,"healthyVolunteers":11,"sex":17,"minAge":58,"maxAge":4,"enrollmentInfo":207,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":209,"conditions":210,"keywords":217,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":223,"lastUpdatePostDateStruct":224,"startDateStruct":226,"completionDateStruct":228,"leadSponsor":230,"locationsCount":50},"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":208,"type":22},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.",[211,212,213,214,215,216,30],"Anesthesia","Gastric Ultrasound","Sonography","Point of Care Ultrasound (POCUS)","Regurgitation","Pulmonary Aspiration During Anesthetic Induction",[218,219,220,221,222],"point of care ultrasound","gastric ultrasound","trauma patients","aspiration","anesthesia","2024-10-14",{"date":225,"type":42},"2024-10-16",{"date":227,"type":42},"2023-02-01",{"date":229,"type":22},"2025-09-30",{"name":231,"class":49},"Kantonsspital Winterthur KSW"]