[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100595311":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":11,"centralContacts":28,"locations":34,"responsibleParty":49,"collaborators":51,"id":54,"slug":55,"hasResults":56,"nctId":57,"briefTitle":58,"officialTitle":58,"acronym":59,"eligibilityCriteria":60,"healthyVolunteers":56,"sex":61,"minAge":62,"maxAge":63,"enrollmentInfo":64,"targetDuration":11,"studyType":67,"phases":68,"briefSummary":70,"conditions":71,"keywords":75,"overallStatus":37,"whyStopped":11,"lastUpdateSubmitDate":79,"lastUpdatePostDateStruct":80,"startDateStruct":83,"completionDateStruct":85,"leadSponsor":87,"locationsCount":88},{"fullName":5,"class":6},"Centre Hospitalier Universitaire, Amiens","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"oxybutynin","ACTIVE_COMPARATOR",null,[13],"Other: Oxybutynin",{"label":15,"type":16,"description":11,"interventionNames":17},"TENS","EXPERIMENTAL",[18],"Device: medical device Urostim",[20,23],{"type":6,"name":21,"description":9,"armGroupLabels":22,"otherNames":11},"Oxybutynin",[9],{"type":24,"name":25,"description":26,"armGroupLabels":27,"otherNames":11},"DEVICE","medical device Urostim","medical device used to deliver posterior tibial nerve stimulation (PTNS)",[15],[29],{"name":30,"role":31,"phone":32,"phoneExt":11,"email":33},"Elodie Haraux, Pr","CONTACT","33+322836787","Haraux.elodie@chu-amiens.fr",[35],{"facility":36,"status":37,"city":38,"state":11,"zip":11,"country":39,"countryCode":40,"cosmosGeoPoint":41,"geoPoint":46,"contacts":47},"CHRU Amiens","RECRUITING","Amiens","France","FR",{"type":42,"coordinates":43},"Point",[44,45],2.3,49.9,{"lat":45,"lon":44},[48],{"name":30,"role":31,"phone":32,"phoneExt":11,"email":33},{"type":50,"investigatorFullName":11,"investigatorTitle":11,"investigatorAffiliation":11,"oldNameTitle":11,"oldOrganization":11},"SPONSOR",[52],{"name":53,"class":6},"University Hospital, Rouen","100595311","comparative-study-of-the-efficacy-of-treatment-of-idiopathic-overactive-bladder-oab-in-children-oxybutynine-vs-transcutaneous-neurostimulation-100595311",false,"NCT07030803","Comparative Study of the Efficacy of Treatment of Idiopathic Overactive Bladder (OAB) in Children: Oxybutynine vs. Transcutaneous Neurostimulation","HAV-O-TENS","Inclusion Criteria:\n\n* Patients aged 6 to 16 years\n* Showing signs of OAB (pollakiuria (\\> 8 micturitions\u002Fd and\u002For urgenturia(\\>x2\u002Fweek) and\u002For daytime urine leakage (1\u002Fd) and\u002For nocturia x2\u002Fnight)\n* No treatment for more than 3 months\n* Urotherapy rules followed for at least 1 month\n* Beneficiary of a social security plan\n* Signature of consent by parents\u002Flegal guardian(s) and child's agreement\n\nExclusion Criteria:\n\n* Neurological cause of bladder dysfunction,\n* History of pelvic surgery,\n* Significant post-micturition residual (\\> 10% of micturition),\n* Recurrent urinary tract infections (\\> 3) in the 6 months prior to inclusion or urinary tract infection at inclusion.\n* Pregnant or breast-feeding adolescents\n* Severe constipation resistant to treatment (Rome IV),\n* Contraindication to oxybutynin\n* Contraindication to the use of TENS (Urostim)","ALL","6 Years","16 Years",{"count":65,"type":66},124,"ESTIMATED","INTERVENTIONAL",[69],"NA","The absence of infectious, urological and neurological causes defines the idiopathic character of overactive bladder (OAB). Although a progressive approach starting with behavioural therapy (urotherapy) is recommended, anticholinergic agents remain the mainstay of medical treatment of overactive bladder (OAB) in children. Bladder neuromodulation is also used but no study with sufficient evidence has assessed its effectiveness and tolerance compared to the reference treatment. The purpose of HAV-O-TENS is to demonstrate the non-inferiority of treating idiopathic overactive bladder (OAB) in children using posterior tibial nerve stimulation (PTNS) compared to the reference treatment with oxybutynin after three months of treatment.\n\nBefore inclusion, patients will receive instructions for urotherapy and a treatment plan. After confirming the diagnosis and obtaining informed consent, patients will be randomly assigned to either oxybutynin or PTNS (posterior tibial nerve stimulation) treatment, and their effectiveness, tolerance, and adherence will be monitored.",[72,73,74],"Overactive Bladder (OAB)","Transcutaneous Neurostimulation","Posterior Tibial Nerve Stimulation",[76,77,78],"Overactive Bladder","transcutaneous neurostimulation","posterior tibial nerve stimulation","2025-11-17",{"date":81,"type":82},"2025-11-18","ACTUAL",{"date":84,"type":82},"2025-11-05",{"date":86,"type":66},"2029-03",{"name":5,"class":6},1]