[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100612144":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":10,"centralContacts":21,"locations":27,"responsibleParty":76,"collaborators":78,"id":89,"slug":90,"hasResults":91,"nctId":92,"briefTitle":93,"officialTitle":93,"acronym":10,"eligibilityCriteria":94,"healthyVolunteers":91,"sex":95,"minAge":96,"maxAge":97,"enrollmentInfo":98,"targetDuration":10,"studyType":101,"phases":10,"briefSummary":102,"conditions":103,"keywords":109,"overallStatus":119,"whyStopped":10,"lastUpdateSubmitDate":120,"lastUpdatePostDateStruct":121,"startDateStruct":124,"completionDateStruct":126,"leadSponsor":128,"locationsCount":129},{"fullName":5,"class":6},"Henry M. Jackson Foundation for the Advancement of Military Medicine","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Group 1 - Minimal Risk Burn Patient",null,"The study includes adult patients (18 years and older) admitted with significant burn injuries involving more than 10% of their total body surface area (TBSA) who require surgical management and\u002For care within a surgical critical care setting. As part of their participation, small amounts of blood are collected at scheduled times during hospitalization, and small pieces of skin or tissue normally removed during burn surgery may also be saved. Medical information already recorded in the hospital chart-such as vital signs, lab results, surgeries, and complications-is also included in the study.",[13],"Other: Observational Cohort (No Intervention)",[15],{"type":6,"name":16,"description":17,"armGroupLabels":18,"otherNames":19},"Observational Cohort (No Intervention)","This is not a treatment trial-no drugs, devices, or procedures are being tested. Participants receive standard burn care only. The research involves collecting blood and tissue samples (when clinically indicated) and reviewing medical record data.",[9],[20],"observational",[22],{"name":23,"role":24,"phone":25,"phoneExt":10,"email":26},"Seth Schobel-McHugh, PhD","CONTACT","(301) 295-3164","seth.schobel-mchugh@usuhs.edu",[28,46,61],{"facility":29,"status":10,"city":30,"state":31,"zip":32,"country":33,"countryCode":34,"cosmosGeoPoint":35,"geoPoint":40,"contacts":41},"University of South Florida - Tampa General Hospital","Tampa","Florida","33606","United States","US",{"type":36,"coordinates":37},"Point",[38,39],-82.45843,27.94752,{"lat":39,"lon":38},[42],{"name":43,"role":24,"phone":44,"phoneExt":10,"email":45},"Jared Troy, MD","832-496-1567","jtroy@usf.edu",{"facility":47,"status":10,"city":48,"state":49,"zip":50,"country":33,"countryCode":34,"cosmosGeoPoint":51,"geoPoint":55,"contacts":56},"Emory University-Grady Memorial Hospital","Atlanta","Georgia","30303",{"type":36,"coordinates":52},[53,54],-84.38798,33.749,{"lat":54,"lon":53},[57],{"name":58,"role":24,"phone":59,"phoneExt":10,"email":60},"Laura Pruskowski, MD","404) 616 - 9852","laura.s.johnson@emory.edu",{"facility":62,"status":10,"city":63,"state":64,"zip":65,"country":33,"countryCode":34,"cosmosGeoPoint":66,"geoPoint":70,"contacts":71},"United States Army Institute of Surgical Research","Houston","Texas","78234",{"type":36,"coordinates":67},[68,69],-95.36327,29.76328,{"lat":69,"lon":68},[72],{"name":73,"role":24,"phone":74,"phoneExt":10,"email":75},"Kaitlin Pruskowski, PharmD","210-438-7024","kaitlin.a.pruskowski.civ@health.mil",{"type":77,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR",[79,82,84,85,87],{"name":80,"class":81},"United States Department of Defense","FED",{"name":83,"class":6},"Emory University",{"name":62,"class":81},{"name":86,"class":6},"University of South Florida",{"name":88,"class":81},"Uniformed Services University of the Health Sciences","100612144","surgical-critical-care-initiative-sc2i-tissue-and-data-acquisition-protocol-tdap-in-burn-patients-improving-the-robustness-and-generalizability-of-post-burn-sepsis-prediction-with-the-post-burn-sepsis-digital-twin-group-1-100612144",false,"NCT07249762","Surgical Critical Care Initiative (SC2i) Tissue and Data Acquisition Protocol (TDAP) in Burn Patients Improving the Robustness and Generalizability of Post-burn Sepsis Prediction With the Post-Burn Sepsis Digital Twin. Group 1","Inclusion Criteria:\n\n* Burn Injury \\>10% TBSA with who have a recognized concurrent or impending risk for clinical decompensation.\n* Male and female ages 18 years and older (maximum age of 80 years old) with burn injury or related illness requiring surgical care or treatment in a critical care or emergency setting who are being cared for at an SC2i-member clinical care facility (Emory\u002FGrady, USF and USAISR) will be considered for study.\n* Ability to understand the purposes and risks of the study and to provide informed consent, either through written documentation or in accordance with the IRB-approved Waiver of Documentation of Consent procedures. In the case of incapacitated patients, a willing Legally Authorized Representative (LAR) may provide informed consent in accordance with written documentation or under the provisions of the approved Waiver of Documentation of Consent.\n\nExclusion Criteria:\n\n* Any condition that, in the opinion of the attending physician, would place the patient or volunteer subject at undue risk by participating. Specific conditions include but are not limited to anemia prohibitive of phlebotomy, or technical considerations that would prevent acquisition of sufficient tissue for clinical use.\n* Pregnant patients\n* Minors \\\u003C 18 years of age\n* Prisoners","ALL","18 Years","80 Years",{"count":99,"type":100},40,"ESTIMATED","OBSERVATIONAL","This study is following adult patients with serious burn injuries to better understand how their bodies respond to treatment and recovery. Researchers will collect small amounts of blood and tissue samples, along with information already recorded in the medical record, such as vital signs, lab results, and details of surgeries or complications. The goal is to identify patterns that may help predict who is at higher risk for infections or other problems after a burn injury. This information could lead to new tools, including computer-based models, to improve burn care and outcomes in the future. Participation involves providing samples and allowing researchers to review medical records during the hospital stay and up to one year after discharge.",[104,105,106,107,108],"Sepsis","Burn Injury","Wound Healing","Critical Illness","Multiple Organ Dysfunction Syndrome",[110,104,107,111,112,113,114,106,115,116,117,118],"Burn Infection","Thermal Injury","Infection","Multiple Organ Dysfunction Syndrome (MODS)","Acute Respiratory Distress Syndrome (ARDS)","Biomarkers","Digital Twin Model","Predictive Analytics","Surgical Critical Care","NOT_YET_RECRUITING","2026-02-02",{"date":122,"type":123},"2026-02-04","ACTUAL",{"date":125,"type":100},"2026-05-15",{"date":127,"type":100},"2027-12-15",{"name":5,"class":6},3]