[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100053238":3},{"organization":4,"armGroups":7,"interventions":24,"overallOfficials":29,"centralContacts":29,"locations":37,"responsibleParty":60,"collaborators":29,"id":64,"slug":65,"hasResults":66,"nctId":67,"briefTitle":68,"officialTitle":69,"acronym":29,"eligibilityCriteria":70,"healthyVolunteers":66,"sex":71,"minAge":72,"maxAge":29,"enrollmentInfo":73,"targetDuration":29,"studyType":76,"phases":77,"briefSummary":79,"conditions":80,"keywords":83,"overallStatus":40,"whyStopped":29,"lastUpdateSubmitDate":93,"lastUpdatePostDateStruct":94,"startDateStruct":97,"completionDateStruct":99,"leadSponsor":101,"locationsCount":102},{"fullName":5,"class":6},"Ege University","OTHER",[8,14,19],{"label":9,"type":10,"description":11,"interventionNames":12},"Acrylic Adhesive Tape","EXPERIMENTAL","Participants will receive central venous catheter securement using an acrylic adhesive tape according to the standardized dressing protocol. Dressing application, assessment, and replacement will be performed following the study protocol throughout catheterization.",[13],"Device: Acrylic Adhesive Tape",{"label":15,"type":10,"description":16,"interventionNames":17},"Silicone Adhesive Tape","Participants will receive central venous catheter securement using a silicone adhesive tape according to the standardized dressing protocol. Dressing application, assessment, and replacement will be performed following the study protocol throughout catheterization.",[18],"Device: Silicone Adhesive Tape",{"label":20,"type":10,"description":21,"interventionNames":22},"Barrier Film + Acrylic Adhesive Tape","Participants will receive a skin barrier film before application of an acrylic adhesive tape for central venous catheter securement according to the standardized dressing protocol. Dressing application, assessment, and replacement will be performed following the study protocol throughout catheterization.",[23],"Device: Skin Barrier Film + Acrylic Adhesive Tape",[25,30,33],{"type":26,"name":9,"description":27,"armGroupLabels":28,"otherNames":29},"DEVICE","A physician will insert a non-tunneled internal jugular central venous catheter using sterile technique and secure the catheter to the skin with sutures according to routine clinical practice. Following skin antisepsis, the insertion site will be covered with sterile 2 × 2 cm gauze and secured with a 10 × 10 cm acrylic adhesive tape. Dressings will be changed every 24 hours or earlier if clinically indicated. Participants will be followed for up to 21 days or until catheter removal, with assessment for medical adhesive-related skin injury (MARSI) at each dressing change.",[9],null,{"type":26,"name":15,"description":31,"armGroupLabels":32,"otherNames":29},"A physician will insert a non-tunneled internal jugular central venous catheter using sterile technique and secure the catheter to the skin with sutures according to routine clinical practice. Following skin antisepsis, the insertion site will be covered with sterile 2 × 2 cm gauze and secured with a 10 × 10 cm silicone adhesive tape. Dressings will be changed every 24 hours or earlier if clinically indicated. Participants will be followed for up to 21 days or until catheter removal, with assessment for medical adhesive-related skin injury (MARSI) at each dressing change.",[15],{"type":26,"name":34,"description":35,"armGroupLabels":36,"otherNames":29},"Skin Barrier Film + Acrylic Adhesive Tape","A physician will insert a non-tunneled internal jugular central venous catheter using sterile technique and secure the catheter to the skin with sutures according to routine clinical practice. Following skin antisepsis, the insertion site will be covered with sterile 2 × 2 cm gauze. A skin barrier film will be applied to the surrounding skin and allowed to dry before securing the dressing with a 10 × 10 cm acrylic adhesive tape. Dressings will be changed every 24 hours or earlier if clinically indicated. Participants will be followed for up to 21 days or until catheter removal, with assessment for medical adhesive-related skin injury (MARSI) at each dressing change.",[20],[38],{"facility":39,"status":40,"city":41,"state":42,"zip":43,"country":44,"countryCode":29,"cosmosGeoPoint":45,"geoPoint":50,"contacts":51},"Afyonkarahisar Health Sciences University Health Practice and Research Center","RECRUITING","Afyonkarahisar","Center","03030","Turkey (Türkiye)",{"type":46,"coordinates":47},"Point",[48,49],30.54333,38.75667,{"lat":49,"lon":48},[52,57],{"name":53,"role":54,"phone":55,"phoneExt":29,"email":56},"Azize Ozdas Gundogan, RN, MSc","CONTACT","+90533 615 36 55","azize.ozdas@afsu.edu.tr",{"name":58,"role":59,"phone":29,"phoneExt":29,"email":29},"Ibrahım Guven Cosgun, MD","PRINCIPAL_INVESTIGATOR",{"type":61,"investigatorFullName":62,"investigatorTitle":63,"investigatorAffiliation":5,"oldNameTitle":29,"oldOrganization":29},"SPONSOR_INVESTIGATOR","Azize Özdaş Gündoğan","PhD Candidate, Department of Fundamentals of Nursing","100053238","medical-adhesive-and-barrier-products-for-preventing-marsi-in-central-venous-catheter-dressings-100053238",false,"NCT07697430","Medical Adhesive and Barrier Products for Preventing MARSI in Central Venous Catheter Dressings","Effect of Medical Adhesive and Skin Barrier Products Used for Central Venous Catheter Dressings on the Development of Medical Adhesive-Related Skin Injury: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Adults aged 18 years or older. Patients admitted to the Chest Diseases Intensive Care Unit who are undergoing insertion of an internal jugular central venous catheter.\n\nCentral venous catheter inserted by a physician using sterile technique in the intensive care unit or operating room.\n\nIntact skin at the catheter insertion site, with no pre-existing skin injury or dermatological disease.\n\nWritten informed consent provided by the participant or a legally authorized representative.\n\nExclusion Criteria:\n\n* Active or congenital dermatological disease. Known allergy or hypersensitivity to the study dressings or skin barrier film. Clinically significant hyperhidrosis. Central venous catheter inserted through a site other than the internal jugular vein (e.g., subclavian or femoral vein).\n\nPatients requiring contact isolation (e.g., scabies) or airborne isolation (e.g., tuberculosis).","ALL","18 Years",{"count":74,"type":75},162,"ESTIMATED","INTERVENTIONAL",[78],"NA","The goal of this clinical trial is to compare three different dressing securement strategies used for central venous catheters (CVCs) to determine which is more effective in preventing medical adhesive-related skin injury (MARSI) among adults admitted to a Chest Diseases Intensive Care Unit.\n\nThe main questions it aims to answer are:\n\nDoes the type of dressing securement affect the occurrence of MARSI? Which dressing securement strategy is most effective in preventing CVC-related MARSI?\n\nResearchers will compare:\n\nacrylic adhesive tape, silicone adhesive tape, and barrier film combined with acrylic adhesive tape to determine which dressing securement strategy provides the best protection against CVC-related MARSI.\n\nParticipants will:\n\nbe randomly assigned to one of the three dressing securement strategies, receive the assigned dressing securement throughout the study period, undergo regular skin assessments for signs of MARSI, and be followed for up to 21 days or until catheter removal.",[81,82],"Medical Adhesive Related Skin Injury","Central Venous Catheter",[84,81,82,85,9,15,86,87,88,89,90,91,92],"MARSI","Central Venous Catheter Dressing","Barrier Film","Intensive Care Unit","Nursing","Skin Injury","Randomized Controlled Trial","medical adhesive tapes","Central venous catheter dressing fixation","2026-07-05",{"date":95,"type":96},"2026-07-13","ACTUAL",{"date":98,"type":96},"2026-06-01",{"date":100,"type":75},"2027-06-01",{"name":62,"class":6},1]