[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100514229":3},{"organization":4,"outcomesModule":7,"designInfo":14,"detailedDescription":17,"studyPopulation":18,"armGroups":19,"interventions":25,"overallOfficials":13,"centralContacts":31,"locations":38,"responsibleParty":54,"collaborators":56,"id":60,"slug":13,"hasResults":61,"nctId":62,"briefTitle":63,"officialTitle":64,"acronym":65,"eligibilityCriteria":66,"healthyVolunteers":61,"sex":67,"minAge":68,"maxAge":13,"enrollmentInfo":69,"targetDuration":13,"studyType":72,"phases":13,"briefSummary":73,"conditions":74,"keywords":13,"overallStatus":41,"whyStopped":13,"lastUpdateSubmitDate":76,"lastUpdatePostDateStruct":77,"startDateStruct":80,"completionDateStruct":82,"leadSponsor":84,"locationsCount":85},{"fullName":5,"class":6},"GCS Ramsay Santé pour l'Enseignement et la Recherche","OTHER",{"primaryOutcomes":8,"secondaryOutcomes":13,"otherOutcomes":13},[9],{"measure":10,"description":11,"timeFrame":12},"Incidence of complications","The primary endpoint was the incidence of procedural complications between Day 0 and Day 30.","30 days",null,{"allocation":13,"interventionModel":13,"interventionModelDescription":13,"primaryPurpose":13,"observationalModel":15,"timePerspective":16,"maskingInfo":13},"COHORT","PROSPECTIVE","This is an observational, prospective, open, non-comparative (single arm), bicentric study.\n\nThis study is aimed at patients with prostate cancer for whom an ambulatory laparoscopic radical prostatectomy has been validated at a multidisciplinary consultation meeting. The possibility of performing this procedure on an outpatient basis is left to the surgeon's discretion, according to well-defined medical procedure criteria.\n\nThis cohort is part of the usual care. The study will observe the incidence and describe the type, number, severity, duration and frequency of procedure-related complications that may arise in the first month post-op of ambulatory Laparoscopic Radical Prostatectomy. For this reason, patient follow-up will stop at 1 month after surgery, during a routine follow-up visit.","This study is aimed at patients with prostate cancer for whom an ambulatory laparoscopic radical prostatectomy has been validated at a multidisciplinary consultation meeting. Ambulatory management is at the surgeon's discretion, according to well-defined medical procedure criteria.",[20],{"label":21,"type":13,"description":22,"interventionNames":23},"ambulatory patient cohort","Patients with prostate cancer for whom an ambulatory laparoscopic radical prostatectomy has been validated at a multidisciplinary consultation meeting.",[24],"Procedure: Laparoscopic radical prostatectomy",[26],{"type":27,"name":28,"description":29,"armGroupLabels":30,"otherNames":13},"PROCEDURE","Laparoscopic radical prostatectomy","Prostate cancer may require laparoscopic radical prostatectomy, a surgical procedure performed under general anaesthetic.",[21],[32],{"name":33,"role":34,"phone":35,"phoneExt":36,"email":37},"Arnaud BALDINI, MD","CONTACT","469001019","+33","docteur.baldini@urolyon-ouest.fr",[39],{"facility":40,"status":41,"city":42,"state":13,"zip":43,"country":44,"countryCode":45,"cosmosGeoPoint":46,"geoPoint":51,"contacts":52},"Clinique de la Sauvegarde","RECRUITING","Lyon","69009","France","FR",{"type":47,"coordinates":48},"Point",[49,50],4.84789,45.74906,{"lat":50,"lon":49},[53],{"name":33,"role":34,"phone":13,"phoneExt":13,"email":37},{"type":55,"investigatorFullName":13,"investigatorTitle":13,"investigatorAffiliation":13,"oldNameTitle":13,"oldOrganization":13},"SPONSOR",[57],{"name":58,"class":59},"Euraxi Pharma","INDUSTRY","100514229",false,"NCT05975775","Outpatient Laparoscopic Radical Prostatectomy","Study of Postoperative Complications After Laparoscopic Outpatient Radical Prostatectomy in Patients With Localized Prostate Cancer","LORP","Inclusion Criteria:\n\n* Male, age ≥ 18 years;\n* Localized prostate cancer;\n* Validation in a multidisciplinary consultation meeting of curative treatment;\n* Scheduled laparoscopic radical prostatectomy;\n* Patient able to understand the information related to the study, to read the information leaflet and to signify his\u002Fher non-opposition or opposition to participating in the study;\n* Membership of a social security scheme;\n* Patient having been informed and having given oral non-opposition.\n\nExclusion Criteria:\n\n* Surgical emergency;\n* Patient not eligible for ambulatory care;\n* Long-term curative anti-coagulant treatment;\n* Resident more than 100km from the clinic;\n* Home alone the first night;\n* Patient under guardianship, curatorship or deprivation of liberty.","MALE","18 Years",{"count":70,"type":71},64,"ESTIMATED","OBSERVATIONAL","The purpose of the study is to evaluate the incidence of surgery-related complications between Day 0 and Day 30.",[75],"Prostate Cancer","2026-03-27",{"date":78,"type":79},"2026-03-30","ACTUAL",{"date":81,"type":79},"2023-10-20",{"date":83,"type":71},"2026-10",{"name":5,"class":6},1]