[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"skin-injury\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:skin-injury":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":30,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":5},"100633228","paraffin-oil-for-preventing-tourniquet-related-skin-lesions-in-upper-extremity-surgery-100633228",false,"NCT07523958","Paraffin Oil for Preventing Tourniquet-Related Skin Lesions in Upper Extremity Surgery","Paraffin Oil for Preventing Tourniquet-Related Skin Lesions in Upper Extremity Surgery (PARA-TOUR RCT)","PARA-TOUR","IInclusion Criteria:\n\n* Age ≥18 years\n* Patients scheduled for elective upper extremity surgery requiring pneumatic tourniquet application\n* ASA physical status I-III\n* Body mass index (BMI) \\\u003C30 kg\u002Fm²\n* Ability to provide informed consent\n* Willingness to participate in the study\n\nExclusion Criteria:\n\n* Age \\\u003C18 years\n* Known dermatological disease or existing skin lesion at the tourniquet application site\n* Allergy or sensitivity to paraffin oil or related substances\n* Severe systemic disease (ASA IV or higher)\n* Obesity (BMI ≥30 kg\u002Fm²)\n* Emergency surgery\n* Patients transferred to intensive care postoperatively\n* Development of major postoperative complications (e.g., hematoma, seroma, nerve injury, significant bleeding)\n* Inability to communicate or comply with study procedures\n* Withdrawal from the study at any time","ALL","18 Years",{"count":20,"type":21},90,"ESTIMATED","INTERVENTIONAL",[24],"NA","This randomized controlled trial aims to evaluate the effectiveness of topical paraffin oil application in preventing tourniquet-related skin lesions in patients undergoing upper extremity surgery. Pneumatic tourniquets are commonly used to provide a bloodless surgical field; however, they may cause skin complications such as erythema, edema, abrasions, blisters, and burns.\n\nIn this study, adult patients undergoing elective upper extremity surgery will be randomly assigned to either an intervention group receiving topical paraffin oil application in addition to routine protective dressing or a control group receiving routine care only. Skin integrity will be assessed immediately after tourniquet removal and at 30 and 60 minutes postoperatively using standardized skin assessment criteria.\n\nThe findings of this study are expected to contribute to the development of effective, simple, and cost-efficient strategies to prevent tourniquet-related skin complications and improve patient safety and postoperative comfort.",[27,28,29],"Pressure Injury","Skin Lesions","Skin Injury",[31,32,33,34,35],"Paraffin Oil","Tourniquet","Upper Extremity Surgery","Skin Injury Prevention","Randomized Controlled Trial","RECRUITING","2026-06-02",{"date":39,"type":40},"2026-06-04","ACTUAL",{"date":42,"type":40},"2026-01-12",{"date":44,"type":21},"2026-07",{"name":46,"class":47},"Istanbul Medipol University Hospital","OTHER"]