[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100578731":3},{"organization":4,"armGroups":7,"interventions":8,"overallOfficials":7,"centralContacts":15,"locations":21,"responsibleParty":37,"collaborators":39,"id":47,"slug":48,"hasResults":49,"nctId":50,"briefTitle":51,"officialTitle":51,"acronym":52,"eligibilityCriteria":53,"healthyVolunteers":49,"sex":54,"minAge":55,"maxAge":7,"enrollmentInfo":56,"targetDuration":7,"studyType":59,"phases":60,"briefSummary":62,"conditions":63,"keywords":67,"overallStatus":24,"whyStopped":7,"lastUpdateSubmitDate":70,"lastUpdatePostDateStruct":71,"startDateStruct":74,"completionDateStruct":76,"leadSponsor":78,"locationsCount":79},{"fullName":5,"class":6},"Centre Hospitalier Universitaire, Amiens","OTHER",null,[9,12],{"type":6,"name":10,"description":11,"armGroupLabels":7,"otherNames":7},"questionnary","On day 1 of an ureteral double J stenting, each participant will receive the first USSQ questionnaire, in the French validated version. This questionnaire will be completed at home, one week after the intervention and returned at the following consultation or hospitalization.",{"type":6,"name":13,"description":14,"armGroupLabels":7,"otherNames":7},"USSQ survey","if the stent is removed less than 6 months later, the second USSQ survey, in the French validated version will be given to the patient when removing the stent. This questionnaire will be completed at home one week after removal of the stent and return to the referent hospital. If the patient does not return the second questionnaire, our team may contact them by phone to complete it.",[16],{"name":17,"role":18,"phone":19,"phoneExt":7,"email":20},"Philippe De Sousa, MD","CONTACT","33+322455775","desousa.philippe@chu-amiens.fr",[22],{"facility":23,"status":24,"city":25,"state":7,"zip":26,"country":27,"countryCode":28,"cosmosGeoPoint":29,"geoPoint":34,"contacts":35},"CHU Amiens-Picardie","RECRUITING","Amiens","80054","France","FR",{"type":30,"coordinates":31},"Point",[32,33],2.3,49.9,{"lat":33,"lon":32},[36],{"name":17,"role":18,"phone":19,"phoneExt":7,"email":20},{"type":38,"investigatorFullName":7,"investigatorTitle":7,"investigatorAffiliation":7,"oldNameTitle":7,"oldOrganization":7},"SPONSOR",[40,42,45],{"name":41,"class":6},"Centre Hospitalier d'Abbeville",{"name":43,"class":44},"Centre Hospitalier Intercommunal de Compiègne-Noyon","OTHER_GOV",{"name":46,"class":6},"University Hospital, Caen","100578731","risk-factors-for-poor-tolerance-of-ureteral-double-j-stent-100578731",false,"NCT06815107","Risk Factors for Poor Tolerance of Ureteral Double-J Stent","ToleJJ","Inclusion Criteria:\n\n* patient over 18 years old\n* patient who need Ureteral Double-J Stenting\n\nExclusion Criteria:\n\n* patient under 18 years old,\n* Iterative change,\n* understanding disorder,\n* inability to answer the questionnaire,\n* refusal of the patient,\n* long-term Ureteral Double-J Stenting (more than 6 month),\n* active cancer.","ALL","18 Years",{"count":57,"type":58},200,"ESTIMATED","INTERVENTIONAL",[61],"NA","The placement of a Ureteral Double-J Stent as an emergency treatment or preparation for endoscopy after Colic nephritis is very frequent. It is often poorly supported, most often by young patients. A rich symptomatology is related to the probe responsible for a limitation of activities that can have a strong socio-economic impact. The objective of this study is the identification of the predictive factors of poor tolerance.",[64,65,66],"Tolerance","Ureteral Double-J Stent","Urinary Symptoms",[65,68,69],"tolerance","urinary symptom","2025-02-04",{"date":72,"type":73},"2025-02-07","ACTUAL",{"date":75,"type":73},"2020-04-15",{"date":77,"type":58},"2026-04",{"name":5,"class":6},1]