[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Laboratoires URGO\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":72},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,44],{"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":27,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":43},"100626835","evaluation-of-the-efficacy-and-tolerance-of-vashe-solution-versus-saline-solution-in-the-treatment-of-venous-or-mixed-leg-ulcers-presenting-inflammatory-signs-suggesting-heavy-bacterial-load-100626835",false,"NCT07440797","EVALUATION OF THE EFFICACY AND TOLERANCE OF VASHE SOLUTION VERSUS SALINE SOLUTION IN THE TREATMENT OF VENOUS OR MIXED LEG ULCERS PRESENTING INFLAMMATORY SIGNS SUGGESTING HEAVY BACTERIAL LOAD","EVALUATION OF THE EFFICACY AND TOLERANCE OF VASHE SOLUTION VERSUS SALINE SOLUTION IN THE TREATMENT OF VENOUS OR MIXED LEG ULCERS PRESENTING INFLAMMATORY SIGNS SUGGESTING HEAVY BACTERIAL LOAD: MULTICENTER, PROSPECTIVE, OPEN-LABEL, RANDOMIZED CONTROLLED TRIAL","Inclusion Criteria:\n\n* Adult patient, at least 18 years of age or older who has provided free, written, and informed consent,\n* Patient who has already worn compression therapy in the past and agrees to wear the two-layer compression system during the whole treatment period,\n* Patient presenting a venous or mixed leg ulcer predominantly of venous origin (ABPI between ≥0.8≤1.3,\n* Leg ulcer presenting at least 3 inflammatory signs (e.g pain, erythema...)\n* Target leg ulcer located at least 3 cm from the edge of another wound.\n\nExclusion Criteria:\n\n* Pregnant or breastfeeding patient,\n* Patient already participating in another clinical trial, except observational trial\n* Patient with epifascial arterial bypass (superficial arterial bypass)\n* Patient suffering from phlegmatia coerulea dolens, septic phlebitis, acute deep vein thrombosis (DVT), defined as the first 10 days from onset of symptoms, or any DVT for which compression is considered by the Investigator to be contraindicated.\n* Patient receiving or having received systemic antibiotics within the ten days prior to inclusion in the investigation, regardless of therapeutic class or indication,\n* Cancerous wound.","ALL","18 Years",{"count":19,"type":20},102,"ESTIMATED","INTERVENTIONAL",[23],"NA","Evaluation of the efficacy (reduction of inflammatory signs suggesting a local infection) and tolerance (emergence and nature of adverse event) of Vashe solution vs Saline solution in the treatment of venous or mixed leg ulcers presenting inflammatory signs suggesting heavy bacterial load",[26],"Venous Leg Ulcer (VLU)",[28,29,30],"venous leg ulcer","inflammatory signs","chronic wound","NOT_YET_RECRUITING","2026-03-02",{"date":34,"type":35},"2026-03-04","ACTUAL",{"date":37,"type":20},"2026-03",{"date":39,"type":20},"2027-03",{"name":41,"class":42},"Laboratoires URGO","INDUSTRY",1,{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":49,"acronym":50,"eligibilityCriteria":51,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":52,"targetDuration":4,"studyType":21,"phases":54,"briefSummary":55,"conditions":56,"keywords":58,"overallStatus":62,"whyStopped":4,"lastUpdateSubmitDate":63,"lastUpdatePostDateStruct":64,"startDateStruct":66,"completionDateStruct":68,"leadSponsor":70,"locationsCount":71},"100585250","efficacy-and-safety-of-light-compression-system-in-the-local-treatment-of-mixed-leg-ulcers-promethee-clinical-investigation-100585250","NCT06899919","Efficacy and Safety of Light Compression System in the Local Treatment of Mixed Leg Ulcers (PROMETHEE Clinical Investigation)","Evaluation of the Efficacy and Safety of Light Compression System Versus Tubular Bandage in the Local Treatment of Mixed Leg Ulcers: a Prospective Open-label RCT","PROMETHEE","Inclusion Criteria:\n\n* Adult patient (≥ 18 years old), having given free, informed and written consent\n* Patient affiliated to a social security scheme\n* Patient agreeing to wear the study compression system daily\n* Patient with an ankle circumference between 18 and 25 cm\n* Target wound: stage C6 \u002F C6r mixed leg ulcer of the CEAP classification with a 0.6≤ ABPI≤0.8 and TABP≥ 50 mm Hg and arterial echo Doppler confirming the mixed nature of the leg ulcer\n* Target wound with an area between 2 and 20 cm2\n* Target wound with age of ≤18 months\n\nCriteria exclusion:\n\n* Patient with a systemic infection not controlled by appropriate antibiotic therapy\n* Patient having presented in the 3 months preceding his inclusion, a deep vein thrombosis\n* Severe arterial pathology, including an Ankle Blood Pressure Index (ABPI) less than 3 months old \\\u003C0.6\n* Patient bedridden or spending less than an hour per day standing\n* Clinically infected target wound\n* Cancerized target wound",{"count":53,"type":20},210,[23],"Evaluation of the efficacy (wound epithelialization and time to closure) and safety (emergence and nature of adverse event) of a lite compression system versus a tubular bandage in the local treatment of mixed leg ulcers: prospective multicenter, randomized controlled, open-label french clinical study",[57],"Leg Ulcers",[59,60,61],"Mixed leg ulcers","Quality of life questionnaire","light compression system","RECRUITING","2025-04-07",{"date":65,"type":35},"2025-04-08",{"date":67,"type":35},"2025-03-29",{"date":69,"type":20},"2027-09-30",{"name":41,"class":42},3,""]