[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"wound-surgical\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:wound-surgical":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,40,69,103],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":4,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":28,"lastUpdatePostDateStruct":29,"startDateStruct":32,"completionDateStruct":34,"leadSponsor":36,"locationsCount":39},"100628301","this-is-a-study-to-find-out-whether-music-therapy-can-reduce-stress-during-wound-care-100628301",false,"NCT07459855","This is a Study to Find Out Whether Music Therapy Can Reduce Stress During Wound Care","Music Therapy to Reduce Stress and Increase Satisfaction in Patients Undergoing Surgical Wound Dressings in the In-hospital Setting: a Randomized Study","Inclusion Criteria:\n\n* Hospitalized patients undergoing wound dressing procedures\n* Age ≥ 18 years\n\nExclusion Criteria:\n\n* Pregnant or lactating women\n* Cognitive impairment or language barriers\n* Severe hearing impairment\n* Clinical instability requiring urgent medical intervention at the time of wound dressing","ALL","18 Years",{"count":19,"type":20},50,"ESTIMATED","INTERVENTIONAL",[23],"NA","This study involves hospitalized patients who need wound dressing procedures. Patients will be assigned by chance to one of two groups. One group will listen to music of their choice during wound care, while the other group will receive standard wound care without music. The investigators will then compare the two groups to see whether listening to music helps reduce stress and improve the experience during the procedure.",[26],"Wound Surgical","RECRUITING","2026-03-03",{"date":30,"type":31},"2026-03-10","ACTUAL",{"date":33,"type":20},"2026-02-11",{"date":35,"type":20},"2026-05-31",{"name":37,"class":38},"Ente Ospedaliero Cantonale, Bellinzona","OTHER",1,{"id":41,"slug":42,"hasResults":11,"nctId":43,"briefTitle":44,"officialTitle":45,"acronym":4,"eligibilityCriteria":46,"healthyVolunteers":47,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":48,"targetDuration":4,"studyType":21,"phases":50,"briefSummary":52,"conditions":53,"keywords":56,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":60,"lastUpdatePostDateStruct":61,"startDateStruct":63,"completionDateStruct":65,"leadSponsor":67,"locationsCount":39},"100539863","phase-4-ostomy-primary-closure-with-01-betainepolyhexanide-wound-irrigation-compared-to-pursestring-closure-100539863","NCT06309368","Ostomy Primary Closure With 0.1% Betaine\u002FPolyhexanide Wound Irrigation Compared to Pursestring Closure","To Close or Not to Close: Surgical Site Infection Rates in Ostomy Primary Closure With 0.1% Betaine\u002FPolyhexanide Wound Irrigation Compared to Conventional Ostomy Closure by Secondary Intention","Inclusion Criteria:\n\n* All patients 18 years or older with an diverting loop ileostomy reversal indication will be enrolled\n* Signed consent\n\nExclusion Criteria:\n\n* Under 18 years old, unable to provide consent, has a parastomal hernia requiring mesh repair, or has an end ileostomy",true,{"count":49,"type":20},84,[51],"PHASE4","The goal of this clinical trial is to compare two types of closure in patients with ostomies that are ready for closure. The main questions it aims to answer are:\n\n1. Surgical site infection rates\n2. Patient quality of life\n3. Time to wound healing\n\nParticipants will undergo either complete ostomy wound closure after washing out the wound with Prontosan, or their ostomy wound will be closed using the Pursestring method, where the wound will be left partially open and allowed to heal from the inside out. Researchers will compare these two groups' outcomes (questions to be answered) as listed above.",[54,26,55],"Surgical Site Infection","Colorectal Disorders",[57,54,58,59],"Ostomy","Primary Closure","Secondary Closure","2025-05-27",{"date":62,"type":31},"2025-06-02",{"date":64,"type":31},"2024-03-14",{"date":66,"type":20},"2029-12",{"name":68,"class":38},"University of Nevada, Las Vegas",{"id":70,"slug":71,"hasResults":11,"nctId":72,"briefTitle":73,"officialTitle":74,"acronym":75,"eligibilityCriteria":76,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":77,"targetDuration":4,"studyType":21,"phases":79,"briefSummary":80,"conditions":81,"keywords":84,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":93,"lastUpdatePostDateStruct":94,"startDateStruct":96,"completionDateStruct":98,"leadSponsor":100,"locationsCount":102},"100514386","propel-2-prophylactic-negative-pressure-wound-therapy-in-laparotomy-wounds-100514386","NCT05977816","PROPEL-2: Prophylactic Negative Pressure Wound Therapy in Laparotomy Wounds","PROPEL-2 Prophylactic Negative Pressure Wound Therapy (NPWT) in Laparotomy Wounds: a Randomised Controlled Trial Comparing Negative Pressure Wound Therapy to Standard Wound Management in Patients Following Midline Laparotomy","PROPEL-2","Inclusion Criteria:\n\n* Aged 18 years or older\n* Patient requires visceral abdominal surgery via a midline laparotomy\n* Patients who can complete questionnaires\n\nExclusion Criteria:\n\n• Patients who are unable to adhere to protocol requirements",{"count":78,"type":20},2000,[23],"Post-operative wound issues in abdominal surgery have a significant impact on patient outcomes. This study is taking place to investigate if Negative Pressure Wound Therapy (NPWT) dressings reduces Surgical Site Infections, post surgical complications and improves scar appearance compared to standard dressings.",[26,82,83],"Wound Infection","Cosmesis",[85,86,87,88,89,90,91,92],"Negative Pressure Wound Therapy","Surgical site Infection","Laparotomy","Post-operative Complications","Abdominal Incision","health economics","POSAS","CoPaQ","2024-10-24",{"date":95,"type":31},"2024-10-26",{"date":97,"type":31},"2023-07-14",{"date":99,"type":20},"2026-07",{"name":101,"class":38},"Royal College of Surgeons, Ireland",11,{"id":104,"slug":105,"hasResults":11,"nctId":106,"briefTitle":107,"officialTitle":108,"acronym":109,"eligibilityCriteria":110,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":111,"targetDuration":4,"studyType":21,"phases":113,"briefSummary":80,"conditions":114,"keywords":115,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":118,"lastUpdatePostDateStruct":119,"startDateStruct":121,"completionDateStruct":123,"leadSponsor":125,"locationsCount":126},"100518031","pinta---prophylactic-incisional-negative-pressure-therapy-for-major-amputations-100518031","NCT06025253","PINTA - Prophylactic Incisional Negative Pressure Therapy for Major Amputations","Prophylactic Single-Use Negative Pressure Wound Therapy Devices for Closed Incision Major Amputations","PINTA","Inclusion Criteria:\n\n* Patients aged 18 years or older;\n* Patients undergoing major lower extremity amputation, including below-knee amputation, through-knee amputation and above-knee amputation, for any indication;\n* Patients with primary closure of the surgical incision using either interrupted or continuous sutures\n\nExclusion Criteria:\n\n* Patients \\\u003C18 years;\n* Women who are pregnant and\u002For breast-feeding;\n* Patients with amputations performed without primary skin closure, including guillotine amputations, amputations deliberately left open for drainage purposes and amputations with soft tissues defects at the stump;\n* Patients with amputations where skin glue is the only means of skin closure\n* Patients with a clinically absent femoral pulse",{"count":112,"type":20},728,[23],[26,82,83],[85,54,88,116,92,117],"Health Economics","WoundQol","2024-10-16",{"date":120,"type":31},"2024-10-18",{"date":122,"type":31},"2024-03-01",{"date":124,"type":20},"2026-12-20",{"name":101,"class":38},7]