[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100658293":3},{"organization":4,"outcomesModule":7,"designInfo":31,"detailedDescription":37,"studyPopulation":30,"armGroups":38,"interventions":45,"overallOfficials":50,"centralContacts":54,"locations":63,"responsibleParty":120,"collaborators":30,"id":122,"slug":123,"hasResults":124,"nctId":125,"briefTitle":126,"officialTitle":127,"acronym":128,"eligibilityCriteria":129,"healthyVolunteers":124,"sex":130,"minAge":131,"maxAge":30,"enrollmentInfo":132,"targetDuration":30,"studyType":135,"phases":136,"briefSummary":137,"conditions":138,"keywords":140,"overallStatus":143,"whyStopped":30,"lastUpdateSubmitDate":144,"lastUpdatePostDateStruct":145,"startDateStruct":148,"completionDateStruct":150,"leadSponsor":152,"locationsCount":153},{"fullName":5,"class":6},"Smith & Nephew, Inc.","INDUSTRY",{"primaryOutcomes":8,"secondaryOutcomes":13,"otherOutcomes":30},[9],{"measure":10,"description":11,"timeFrame":12},"Cumulative Incidence of Any Sacral Hospital-Acquired Pressure Injury Through Day 7","The cumulative incidence of sacral hospital-acquired pressure injury (HAPI) is defined as the proportion of participants who developed any qualifying sacral HAPI up to and including Day 7 of study dressing application. A sacral skin assessment will be performed to determine whether any sacral HAPI has developed. \"Yes\" indicates detection of a sacral HAPI classified as Stage 1, Stage 2, Stage 3, Stage 4, unstageable pressure injury, or deep tissue pressure injury. \"No\" indicates the participant did not develop sacral HAPI by Day 7 or discontinued the study before Day 7 without developing sacral HAPI and was therefore considered event-free. Fewer pressure injuries indicate a better outcome.","Day 0 to Day 7",[14,17,20,24,27],{"measure":15,"description":16,"timeFrame":12},"Cumulative Incidence of Sacral Hospital-Acquired Pressure Injury: Stage 2-4, Unstageable, and\u002For Deep Tissue Pressure Injury Through Day 7","The cumulative incidence of sacral hospital-acquired pressure injury (HAPI) is defined as the proportion of participants who developed a stage 2-4, unstageable, or deep tissue HAPI up to and including Day 7 of study dressing application. A sacral skin assessment will be performed to determine whether a qualifying sacral HAPI developed. \"Yes\" indicates detection of a sacral HAPI classified as Stage 2, Stage 3, Stage 4, unstageable pressure injury, or deep tissue pressure injury. \"No\" indicates the participant did not develop a qualifying sacral HAPI by Day 7 or discontinued the study before Day 7 without developing a qualifying sacral HAPI and was therefore considered event-free. Fewer pressure injuries indicate a better outcome.",{"measure":18,"description":19,"timeFrame":12},"Cumulative Incidence of Each Sacral Hospital-Acquired Pressure Injury: Stage 1-4, Unstageable, and\u002For Deep Tissue Pressure Injury Through Day 7","The cumulative incidence of sacral hospital-acquired pressure injury (HAPI) defined as the proportion of participants who developed stage 1-4, unstageable, or deep tissue HAPI up to and including Day 7 of study dressing application. A sacral skin assessment will be performed to determine whether a qualifying sacral HAPI developed. The sacral skin assessment will be categorized as one of the following:\n\n* Stage 1: Non-blanchable erythema of intact skin Intact skin\n* Stage 2: Partial-thickness skin loss with exposed dermis\n* Stage 3: Full-thickness skin loss in which adipose (fat) is visible\n* Stage 4: Full-thickness skin and tissue loss\n* Unstageable: Obscured full-thickness skin and tissue loss\n* Deep Tissue: Intact or non-intact skin with localized area of persistent non-blanchable deep red, maroon or purple discoloration",{"measure":21,"description":22,"timeFrame":23},"Number of Days to Clinical Diagnosis of Sacral Hospital-Acquired Pressure Injury (HAPI)","For participants that develop a sacral hospital-acquired pressure injury (HAPI), the number of days from study dressing application on Day 0 to the clinical diagnosis of sacral HAPI will be summarized.","Day 0 to Day 14",{"measure":25,"description":26,"timeFrame":23},"Dressing Utilization","Dressing utilization will be summarized by the number of dressing changes throughout the treatment period, approximately 14 days.",{"measure":28,"description":29,"timeFrame":23},"Dressing Wear Time","The duration of study dressing wear will be summarized as the total number of days the study dressing was worn during each 7-day period.",null,{"allocation":32,"interventionModel":33,"interventionModelDescription":30,"primaryPurpose":34,"observationalModel":30,"timePerspective":30,"maskingInfo":35},"NA","SINGLE_GROUP","PREVENTION",{"masking":36,"maskingDescription":30,"whoMasked":30},"NONE","Hospital-acquired pressure injuries (also known as pressure ulcers or bed sores) remain a common issue for patients confined to beds in hospitals. This study will see whether the use of a particular foam dressing (ALLEVYN◊ COMPLETE CARE Sacrum) in combination with standard pressure injury prevention protocols will reduce pressure injuries development compared to known rates of pressure injuries for adults receiving critical or intermediate hospital care. Participants will have the study dressing applied to the lower back\u002Ftailbone area, in addition to hospital standard methods used, to try to prevent pressure injuries. Study participation will last up to 14 days. Additional assessments will evaluate the severity and timing of any pressure injuries that occur, dressing utilization, clinician satisfaction with the dressing, dressing wear characteristics, health economic outcomes, and the relationship between pressure injury occurrence, skin tone and other risk factors.",[39],{"label":40,"type":41,"description":42,"interventionNames":43},"ALLEVYN◊ COMPLETE CARE Sacrum","EXPERIMENTAL","ALLEVYN◊ COMPLETE CARE Sacrum as preventative measure for hospital-acquired pressure injuries",[44],"Device: ALLEVYN◊ COMPLETE CARE Sacrum",[46],{"type":47,"name":40,"description":48,"armGroupLabels":49,"otherNames":30},"DEVICE","ALLEVYN◊ COMPLETE CARE Sacrum foam dressing",[40],[51],{"name":52,"affiliation":5,"role":53},"Amanda Spitzer, MBA, RN","STUDY_CHAIR",[55,60],{"name":56,"role":57,"phone":58,"phoneExt":30,"email":59},"Jay Dobson","CONTACT","206-495-7058","Jay.Dobson@smith-nephew.com",{"name":61,"role":57,"phone":30,"phoneExt":30,"email":62},"Laura Everson","Laura.Everson@smith-nephew.com",[64,86,103],{"facility":65,"status":30,"city":66,"state":67,"zip":68,"country":69,"countryCode":70,"cosmosGeoPoint":71,"geoPoint":76,"contacts":77},"VA Western Colorado Health Care System","Grand Junction","Colorado","81501","United States","US",{"type":72,"coordinates":73},"Point",[74,75],-108.55065,39.06387,{"lat":75,"lon":74},[78,83],{"name":79,"role":57,"phone":80,"phoneExt":81,"email":82},"Marty Jacobson","910-242-0731","2153","marty.jacobson@va.gov",{"name":84,"role":85,"phone":30,"phoneExt":30,"email":30},"Eric Hanly, MD","PRINCIPAL_INVESTIGATOR",{"facility":87,"status":30,"city":88,"state":89,"zip":90,"country":69,"countryCode":70,"cosmosGeoPoint":91,"geoPoint":95,"contacts":96},"Grady Memorial Hospital","Atlanta","Georgia","30303",{"type":72,"coordinates":92},[93,94],-84.38798,33.749,{"lat":94,"lon":93},[97,101],{"name":98,"role":57,"phone":99,"phoneExt":30,"email":100},"Katherine Bachman","404-251-0637","katherine.bachman@emory.edu",{"name":102,"role":85,"phone":30,"phoneExt":30,"email":30},"Laura Johnson, MD",{"facility":104,"status":30,"city":105,"state":106,"zip":107,"country":69,"countryCode":70,"cosmosGeoPoint":108,"geoPoint":112,"contacts":113},"Indiana University Health University Hospital","Indianapolis","Indiana","46202",{"type":72,"coordinates":109},[110,111],-86.15804,39.76838,{"lat":111,"lon":110},[114,118],{"name":115,"role":57,"phone":116,"phoneExt":30,"email":117},"Heather Adams","317-962-1130","hadams3@iuhealth.org",{"name":119,"role":85,"phone":30,"phoneExt":30,"email":30},"Terrie Beeson, MSN",{"type":121,"investigatorFullName":30,"investigatorTitle":30,"investigatorAffiliation":30,"oldNameTitle":30,"oldOrganization":30},"SPONSOR","100658293","sacrum-pressure-injury-prevention-study-using-allevyn-complete-care-in-adults-at-risk-of-developing-hospital-acquired-pressure-injuries-in-critical-care-units-100658293",false,"NCT07849387","Sacrum Pressure Injury Prevention Study Using ALLEVYN◊ Complete Care in Adults at Risk of Developing Hospital-acquired Pressure Injuries in Critical Care Units","An Evaluation of Hospital-Acquired Pressure Injury Prevention Using ALLEVYN COMPLETE CARE Sacrum Foam Dressing - A Prospective, Single-Arm Trial (Project Name - PACCT)","PACCT","Inclusion Criteria:\n\n* Subject or legally authorized representative (LAR) provides written informed consent\n* Adults (≥18 years) at time of consent\n* Willing and able to complete all required study visits\n* Subjects admitted to Critical Care Units or Intermediate Care Units (may also be called step-down, progressive care, or high dependency units). Subjects may be identified in perioperative or emergency departments before moving to the appropriate unit.\n* Subject's Braden Scale score is ≤18 at time of screening\n* Subject is recruited within 18 hours of arrival to hospital (Emergency Department, perioperative area or Critical or Intermediate Care Units)\n* Subjects' life expectancy is ≥3 days (as assessed by clinical judgment within 24 hours of consent)\n* Subjects expected Critical and\u002For Intermediate Care stay is ≥3 days (clinical judgment)\n\nExclusion Criteria:\n\n* Subject has participated previously in this clinical trial\n* Subject is currently participating in or has participated in a clinical trial within thirty (30) calendar days of day 0 which could impact the scientific integrity of the study\n* Subject has a medical or physical condition that, in the opinion of the Investigator, would preclude safe participation in the study.\n* Subject has a known sensitivity\u002Fallergy to dressing and\u002For adhesive components (e.g., sensitivity to silicone)\n* Subject has a medical condition or orders that, in the opinion of the Investigator, prevent repositioning (e.g., hemodynamic instability or unstable spine) or positioning which would exclude the supine position (e.g., prone positioning) (clinical judgment)\n* Subjects with orders for, or expected to receive orders for, prone positioning (clinical judgment)\n* Known extended period, prior to enrolment, without documented repositioning in the opinion of the Investigator. e.g., Subject has had ≥6 hours of known pressure on the sacral area, subject found down, extended operating time etc.\n* Subject is currently receiving end-of-life care or comfort care only\n* Subject has existing sacral skin injury or has irregular skin features (e.g., tattoos, pre-existing scarring, evidence of prior healed pressure injury, unusual anatomy such as dimples or bony prominences) which in the opinion of the Investigator, will interfere with the study assessments.\n* Subject has uncontrolled\u002Funmitigated urinary and\u002For fecal incontinence (e.g., controlled defined as incontinence reasonably managed through the use of a device such as indwelling catheter, fecal management system, external urinary catheter, etc.)","ALL","18 Years",{"count":133,"type":134},330,"ESTIMATED","INTERVENTIONAL",[32],"The purpose of this study is to investigate the use of ALLEVYN◊ COMPLETE CARE Sacrum dressing for the prevention of hospital-acquired pressure injuries in adults. The main question it aims to answer is whether or not the dressing will prevent pressure injury prevention between application and Day 7. Participants will apply a dressing to the lower back\u002Ftailbone area as part of their regular care up to 14 days and participate in ongoing checkups by the study team.",[139],"Pressure Ulcers (Hospital-acquired Pressure Injuries)",[141,142],"Pressure injury prevention","Hospital-acquired pressure injury","NOT_YET_RECRUITING","2026-09-24",{"date":146,"type":147},"2026-09-30","ACTUAL",{"date":149,"type":134},"2026-10-30",{"date":151,"type":134},"2028-11-07",{"name":5,"class":6},3]