[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Feeltect Limited\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":70},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,42],{"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":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":31,"startDateStruct":34,"completionDateStruct":36,"leadSponsor":38,"locationsCount":41},"100613583","assessing-sensor-guided-compression-therapy-for-venous-leg-ulcers-healing-outcomes-100613583",false,"NCT07268482","Assessing Sensor-Guided Compression Therapy for Venous Leg Ulcers Healing Outcomes","Randomised Control Study of Using a Pressure Monitoring Technology for Improving the Targeted Application, Monitoring, and Maintenance of Compression Therapy in Patients With Venous Leg Ulcers","Inclusion Criteria:\n\n* Adults with chronic venous leg ulcers (≥6-week and ≤5-year durations) currently in compression therapy treatment.\n* Between 5 and 100 cm2 wound area at randomization.\n* Ankle brachial pressure index (ABPI) of \\>0,8\n* Capable of using use a smart device.\n\nExclusion Criteria:\n\n* Uncontrolled diabetes \\[haemoglobin A1c (HbA1c) ≥12% in the last 3 months\\]\n* Index ulcer has active infection on day of inclusion requiring systemic antibiotic therapy\n* Renal failure\n* Exposed tendon, ligament, muscle or bone in the index ulcer\n* Osteomyelitis, cellulitis or gangrene in study limb\n* Subjects with an amputation above transmetatarsal in study limb\n* Active malignancy affecting study limb\n* Index ulcer is of arterial aetiology (ABPI \\\u003C0.8)\n* Pregnant or breast-feeding women or women of childbearing potential not willing to use a method of highly effective contraception for the duration of the study\n* Planned vascular surgery, angioplasty or thrombolysis procedures during study period. Or patients who are within six weeks of having had such a procedure\n* Planned surgical procedure during study period for the index wound\n* Prior skin replacement, negative-pressure therapy and ultrasound therapy to the study wound in the two weeks before screening\n* Currently receiving or has received radio or chemotherapy within three months of randomisation\n* Index wound would require ultrasound near an electronic implant or prosthesis\n* Not capable of providing informed consent\n* Currently enrolled in or has been enrolled in another investigation device or drug trial in the last 30 days","ALL","18 Years",{"count":19,"type":20},40,"ESTIMATED","INTERVENTIONAL",[23],"NA","The investigators are conducting a study to find out if a new system can help improve the care of people with venous leg ulcers (VLU). Venous leg ulcers are wounds on the lower leg that need compression bandages to help them heal.\n\nIn this study, patients will be randomly placed into one of two groups:\n\n* Group 1: Will receive the usual care for VLUs.\n* Group 2: Will use a new connected health system, called Tight Alright, along with their usual care.\n\nThe Tight Alright system includes a small, wearable device that sits under a patient's bandage. This device measures the pressure at three points on the patient's lower leg and sends the information wirelessly to a mobile app. The app shows real-time pressure readings and also sends the data to a secure cloud database. This allows the patient's healthcare team to monitor their bandage pressure remotely and make sure it is just right.\n\nThe aim is to help nurses and doctors apply the correct pressure every time, which is important for healing. The system can also alert the patient's healthcare team if the pressure drops, so they can decide if a patient's bandage needs adjusting, even when the patient is at home.\n\nThe investigators will follow all participants for 90 days and then compare how well the ulcers have healed in both groups. This will help us find out if the new system can improve healing and make treatment safer and more effective.",[26],"Venous Leg Ulcer (VLU)",[28],"Venous Leg Ulcers","NOT_YET_RECRUITING","2025-11-25",{"date":32,"type":33},"2025-12-05","ACTUAL",{"date":35,"type":20},"2026-01-15",{"date":37,"type":20},"2026-10-30",{"name":39,"class":40},"Feeltect Limited","INDUSTRY",1,{"id":43,"slug":44,"hasResults":11,"nctId":45,"briefTitle":46,"officialTitle":47,"acronym":48,"eligibilityCriteria":49,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":50,"targetDuration":4,"studyType":21,"phases":51,"briefSummary":52,"conditions":53,"keywords":55,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":62,"lastUpdatePostDateStruct":63,"startDateStruct":65,"completionDateStruct":67,"leadSponsor":69,"locationsCount":41},"100604684","assessing-connected-health-pressure-monitoring-technology-for-improving-compression-therapy-in-venous-leg-ulcer-treatment-100604684","NCT07152717","Assessing Connected-Health, Pressure-Monitoring Technology for Improving Compression Therapy in Venous Leg Ulcer Treatment","Assessment of a Connected-health, Pressure Monitoring Technology for Improving Clinical Outcomes of Compression Therapy in the Treatment of Venous Leg Ulcers","ACHIEVE","Inclusion Criteria:\n\n* Patient of Parkview Noble Center for Wound Healing\n* Adults 18+ with venous leg ulcers receiving compression therapy treatment prescribed by outpatient wound clinic.\n* Capable of using use a smart device\n* Owns a smart phone or device capable of downloading the Mobile App\n\nExclusion Criteria:\n\n* \\\u003C18 years old\n* Unable to consent in English\n* Cellulitis in affected limb\n* Acute deep vein thrombosis in affected limb\n* Active malignancy in affected limb\n* Prisoners\n* Currently enrolled in or has been enrolled in another investigation device or drug trial in the last 30 days",{"count":19,"type":20},[23],"This study evaluates the effectiveness of a connected-health, pressure monitoring technology (Tight Alright) to improve clinical outcomes of compression therapy in patients with venous leg ulcers (VLUs). Compression therapy is the standard of care for VLUs, but achieving and maintaining therapeutic sub-bandage pressure is challenging due to patient variability and lack of objective feedback. The Tight Alright system includes a wearable device that measures sub-bandage pressure at multiple points on the leg and transmits data to a mobile app and cloud database, enabling both guided compression application at the point-of-care and guided compression maintenance via remote monitoring.\n\nThe study will be conducted at Parkview Noble Center for Wound Healing and will include two cohorts: a control group receiving standard unguided compression therapy with blinded device use (i.e. compression pressures will be blinded at the point of care but monitored remotely), and an intervention group using Tight Alright technology to guide compression application and reapplication. Outcomes will include wound healing rates, time to healing, pressure maintenance, patient adherence, and usability. The study aims to determine whether integrating connected-health pressure monitoring can improve consistency of compression therapy, accelerate healing, and enhance patient engagement in the treatment of venous leg ulcers",[54],"Venous Leg Ulcers (VLUs)",[56,57,58,59,60,61],"wound care","compression therapy","venous leg ulcers","remote monitoring","pressure sensing","connected health","2025-08-26",{"date":64,"type":33},"2025-09-03",{"date":66,"type":20},"2025-10-01",{"date":68,"type":20},"2026-12-31",{"name":39,"class":40},""]