[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"female-urinary-incontinence\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:female-urinary-incontinence":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,51],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":29,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":39,"lastUpdatePostDateStruct":40,"startDateStruct":43,"completionDateStruct":45,"leadSponsor":47,"locationsCount":50},"100587135","effect-of-modified-mesh-on-surgical-success-in-transobturator-tape-surgery-100587135",false,"NCT06924450","Effect of Modified Mesh on Surgical Success in Transobturator Tape Surgery","MOTOT","Inclusion Criteria:\n\n* Female patients aged 18 years or older\n* Clinical diagnosis of stress urinary incontinence (SUI), confirmed by:\n* Positive stress test (urine leakage on coughing with a comfortably full bladder)\n* Q-tip test showing urethral hypermobility (\\>30 degrees)\n* Inadequate response to conservative therapy (e.g., pelvic floor muscle training, behavioral therapy)\n* Eligible for transobturator tape (TOT) surgery\n* Body mass index (BMI) less than 35 kg\u002Fm²\n* Able to provide informed consent and follow postoperative instructions\n\nExclusion Criteria:\n\n* History of prior midurethral sling surgery\n* Mixed urinary incontinence or urge-dominant symptoms\n* Pelvic organ prolapse stage \\> II according to the POP-Q system\n* Neurological disorders affecting bladder function (e.g., multiple sclerosis, spinal cord injury)\n* Active urinary tract infection or recurrent UTI (defined as ≥3 infections within the past 12 months)\n* Pregnant or planning to become pregnant within the next 12 months\n* Severe comorbid conditions (e.g., uncontrolled diabetes mellitus, active malignancy, pelvic radiotherapy)\n* Use of medications that significantly affect bladder function (e.g., anticholinergics, diuretics)\n* Inability or unwillingness to attend follow-up visits or comply with postoperative care plan","FEMALE","18 Years",{"count":19,"type":20},106,"ESTIMATED","INTERVENTIONAL",[23],"NA","This study is a single-blind, randomized controlled trial evaluating whether changing the width of the surgical tape (mesh) used in transobturator tape (TOT) surgery improves treatment results in women with stress urinary incontinence (SUI). Two mesh widths are being compared: a 1.2 cm mesh (new method) and a 1.0 cm mesh (standard method). The main goal is to find out if the wider mesh leads to better urinary control and fewer complications. Participants will be followed for one year to measure cure rates, symptom improvement, and satisfaction.",[26,27,28],"Stress Urinary Incontinence","Female Urinary Incontinence","Pelvic Floor Dysfunction",[30,31,32,33,34,35,36,37],"Urinary Incontinence","Stress Urinary Incontinence (SUI)","Female Pelvic Health","Transobturator Tape (TOT) Procedure","Pelvic Floor Surgery","Surgical Mesh","Randomized Controlled Trial","Urogynecology","RECRUITING","2025-07-08",{"date":41,"type":42},"2025-07-11","ACTUAL",{"date":44,"type":42},"2025-05-12",{"date":46,"type":20},"2025-11-12",{"name":48,"class":49},"Izzet Celegen","OTHER",1,{"id":52,"slug":53,"hasResults":11,"nctId":54,"briefTitle":55,"officialTitle":56,"acronym":4,"eligibilityCriteria":57,"healthyVolunteers":58,"sex":16,"minAge":59,"maxAge":60,"enrollmentInfo":61,"targetDuration":4,"studyType":63,"phases":4,"briefSummary":64,"conditions":65,"keywords":4,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":67,"startDateStruct":69,"completionDateStruct":71,"leadSponsor":73,"locationsCount":75},"100538484","women-urinary-incontinence-prevalence-study-wuips-100538484","NCT06291441","Women Urinary Incontinence Prevalence Study (WUIPS)","Female Urinary Incontinence in Middle-aged Women in Four Hospitals in Northern Italy: a Multicenter Prevalence Study","INCLUSION CRITERIA\n\n* Female sex\n* Middle age (40-65 years old)\n* Informed consent signed\n* Comprehension of written and spoken Italian language\n* Female outpatients intended for any hospital unit (outpatient clinic, day surgery and day hospital patients included) and every female caregiver respecting the previous inclusion criteria, recruited at the central admission and at the private admission of the four hospitals involved\n* Female workers (healthcare professionals and administrative personnel) of the four hospitals\n\nEXCLUSION CRITERIA\n\n* Male sex\n* Young age (\\\u003C 40 years) and older age (\\> 65 years)\n* Pregnant women\n* Puerperium women (up to 40 days post-partum)\n* Women who had undergone urinary and gynecology surgery",true,"40 Years","65 Years",{"count":62,"type":20},449,"OBSERVATIONAL","The goal of this multicenter prospective and prevalence observational study is to punctually investigate and describe prevalence, predictors, quality of life and costs of Urinary Incontinence (UI) among female patients, female caregivers and female personnel in four hospitals in Northern Italy: San Raffaele hospital in Milan, San Raffaele Turro hospital in Milan, Zingonia Policlinico San Marco (BG) and Policlinico San Pietro in Ponte San Pietro (BG).",[27],"2024-09-14",{"date":68,"type":42},"2024-09-19",{"date":70,"type":42},"2024-07-03",{"date":72,"type":20},"2025-12-31",{"name":74,"class":49},"IRCCS San Raffaele",4]