[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100645821":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","100645821","medical-adhesive-and-barrier-products-for-preventing-marsi-in-central-venous-catheter-dressings-100645821",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* Patients aged 18 years or older.\n* Patients scheduled to undergo insertion of a non-tunneled central venous catheter via the internal jugular vein in the chest intensive care unit or operating room.\n* Patients who provide written informed consent to participate in the study, either personally or through their legally authorized representative.\n* Patients with intact skin and no pre-existing skin condition at the catheter insertion site.\n\nExclusion Criteria:\n\n* Patients with an active or congenital dermatological disease.\n* Patients with a known history of allergic reactions to any of the securement products used in the study (medical adhesive tapes or protective barrier film).\n* Patients with clinically significant hyperhidrosis (excessive sweating).\n* Patients whose central venous catheter is inserted through a site other than the internal jugular vein (e.g., subclavian or femoral vein).\n* Patients requiring contact isolation because of an infectious disease (e.g., scabies) or airborne isolation because of a contagious disease (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","2026-07-19",{"date":95,"type":96},"2026-07-21","ACTUAL",{"date":98,"type":96},"2026-06-01",{"date":100,"type":75},"2027-06-01",{"name":62,"class":6},1]