[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100640354":3},{"organization":4,"armGroups":7,"interventions":25,"overallOfficials":24,"centralContacts":32,"locations":24,"responsibleParty":38,"collaborators":24,"id":41,"slug":42,"hasResults":43,"nctId":44,"briefTitle":45,"officialTitle":46,"acronym":24,"eligibilityCriteria":47,"healthyVolunteers":43,"sex":48,"minAge":49,"maxAge":24,"enrollmentInfo":50,"targetDuration":24,"studyType":53,"phases":54,"briefSummary":56,"conditions":57,"keywords":59,"overallStatus":64,"whyStopped":24,"lastUpdateSubmitDate":65,"lastUpdatePostDateStruct":66,"startDateStruct":69,"completionDateStruct":71,"leadSponsor":73,"locationsCount":24},{"fullName":5,"class":6},"Hacettepe University","OTHER",[8,14,20],{"label":9,"type":10,"description":11,"interventionNames":12},"Group 1","EXPERIMENTAL","Use of silicone foam dressing and repositioning every 8 hours",[13],"Other: Use of silicone foam dressing and repositioning every 8 hours",{"label":15,"type":16,"description":17,"interventionNames":18},"Group 2","ACTIVE_COMPARATOR","Repositioning every 8 hours",[19],"Other: Repositioning every 8 hours",{"label":21,"type":22,"description":23,"interventionNames":24},"Group 3","NO_INTERVENTION","Standard care (Control Group)",null,[26,29],{"type":6,"name":11,"description":27,"armGroupLabels":28,"otherNames":24},"Patients assigned to this group will receive a silicone foam dressing applied over the endotracheal tube, with repositioning performed every 8 hours. As the silicone foam wound dressing, AQUACEL™ Foam, a sterile, waterproof dressing consisting of a polyurethane outer film layer and a multilayer absorbent pad with silicone adhesive borders, will be used.",[9],{"type":6,"name":17,"description":30,"armGroupLabels":31,"otherNames":24},"In patients assigned to this group, the initial repositioning following intubation and the first assessment of the lips, oral cavity, and perioral skin and mucosa will be performed 8 hours after intubation. If the endotracheal tube (ETT) is positioned at the right or left corner of the mouth, it will be repositioned to the midline; if it is positioned at the midline, it will be repositioned to either the right or left corner of the mouth. Following the initial repositioning, subsequent repositioning procedures will be performed every 8 hours.",[15],[33],{"name":34,"role":35,"phone":36,"phoneExt":24,"email":37},"Cansu CAMBAZ","CONTACT","+9 0312 305 15 80","cansuyildizoglu65@gmail.com",{"type":39,"investigatorFullName":34,"investigatorTitle":40,"investigatorAffiliation":5,"oldNameTitle":24,"oldOrganization":24},"PRINCIPAL_INVESTIGATOR","Research Assistant","100640354","the-effect-of-silicone-foam-dressing-and-repositioning-on-the-prevention-of-endotracheal-tube-related-pressure-injuries-100640354",false,"NCT07608484","The Effect of Silicone Foam Dressing and Repositioning on the Prevention of Endotracheal Tube-related Pressure Injuries","The Effect of Silicone Foam Dressing and Repositioning on the Prevention of Endotracheal Tube-related Pressure Injuries: A Randomized Comparative Study","Inclusion Criteria:\n\n* Aged 18 years or older\n* Patients admitted to the General Intensive Care Unit and receiving mechanical ventilation support\n* Absence of pressure injuries, other lesions, or anomalies on the inner and outer surfaces of the lips and at the oral commissures prior to intubation\n* Absence of congenital anomalies that could interfere with the assessment of pressure injuries on the inner and outer surfaces of the lips and at the oral commissures\n\nExclusion Criteria:\n\n* Receiving mechanical ventilation support initiated prior to admission to the intensive care unit\n* Undergoing nasotracheal intubation\n* History of any intraoral surgical procedure\n* Presence of a contraindication to repositioning of the endotracheal tube\n* More than one hour having elapsed since intubation (for Group 1)","ALL","18 Years",{"count":51,"type":52},75,"ESTIMATED","INTERVENTIONAL",[55],"NA","The endotracheal tube is one of the medical devices most associated with pressure injuries related to medical devices. This study aims to evaluate the effectiveness of applying a silicone foam dressing over the endotracheal tube and repositioning the endotracheal tube in preventing endotracheal tube-related pressure injuries in patients receiving mechanical ventilation support.",[58],"Pressure Injury Prevention",[60,61,62,63],"Pressure injury","Intensive care unit","Endotracheal tube","Prevention","NOT_YET_RECRUITING","2026-05-30",{"date":67,"type":68},"2026-06-02","ACTUAL",{"date":70,"type":52},"2026-06-01",{"date":72,"type":52},"2027-08-30",{"name":5,"class":6}]