[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100658308":3},{"organization":4,"outcomesModule":7,"designInfo":18,"detailedDescription":17,"studyPopulation":21,"armGroups":22,"interventions":30,"overallOfficials":17,"centralContacts":35,"locations":42,"responsibleParty":61,"collaborators":17,"id":63,"slug":64,"hasResults":65,"nctId":66,"briefTitle":67,"officialTitle":68,"acronym":69,"eligibilityCriteria":70,"healthyVolunteers":65,"sex":71,"minAge":72,"maxAge":17,"enrollmentInfo":73,"targetDuration":76,"studyType":77,"phases":17,"briefSummary":78,"conditions":79,"keywords":81,"overallStatus":84,"whyStopped":17,"lastUpdateSubmitDate":85,"lastUpdatePostDateStruct":86,"startDateStruct":89,"completionDateStruct":91,"leadSponsor":93,"locationsCount":94},{"fullName":5,"class":6},"University Hospital, Toulouse","OTHER",{"primaryOutcomes":8,"secondaryOutcomes":13,"otherOutcomes":17},[9],{"measure":10,"description":11,"timeFrame":12},"Evaluation of obstetric outcomes","vaginal delivery rate","6 days after the inclusion",[14],{"measure":15,"description":16,"timeFrame":12},"Evaluation of postpartum patient satisfaction","Satisfaction survey",null,{"allocation":17,"interventionModel":17,"interventionModelDescription":17,"primaryPurpose":17,"observationalModel":19,"timePerspective":20,"maskingInfo":17},"COHORT","PROSPECTIVE","pregnant patients with an indication for balloon induction",[23,27],{"label":24,"type":17,"description":17,"interventionNames":25},"Pregnant patients undergoing balloon induction and returning home",[26],"Other: Questionnaire and Physical Exam",{"label":28,"type":17,"description":17,"interventionNames":29},"Pregnant patients undergoing balloon induction in a standard hospital setting",[26],[31],{"type":6,"name":32,"description":33,"armGroupLabels":34,"otherNames":17},"Questionnaire and Physical Exam","A satisfaction questionnaire is given to the patient during her stay at the maternity ward.",[24,28],[36],{"name":37,"role":38,"phone":39,"phoneExt":40,"email":41},"Thomas PARSY","CONTACT","05 67 77 12 31","+33","parsy.t@chu-toulouse.Fr",[43],{"facility":44,"status":17,"city":45,"state":46,"zip":47,"country":48,"countryCode":49,"cosmosGeoPoint":50,"geoPoint":55,"contacts":56},"Service de gynécologie, Hôpital Paule de Viguier","Toulouse","Oui","31000","France","FR",{"type":51,"coordinates":52},"Point",[53,54],1.44367,43.60426,{"lat":54,"lon":53},[57],{"name":58,"role":38,"phone":59,"phoneExt":40,"email":60},"Emeline Muller","0561778707","muller.E@chu-toulouse.Fr",{"type":62,"investigatorFullName":17,"investigatorTitle":17,"investigatorAffiliation":17,"oldNameTitle":17,"oldOrganization":17},"SPONSOR","100658308","comparative-analysis-of-labor-induction-using-a-balloon-catheter-at-home-versus-in-the-hospital-100658308",false,"NCT07848412","Comparative Analysis of Labor Induction Using a Balloon Catheter at Home Versus in the Hospital","Comparative Prospective Analysis of Labor Induction Using a Balloon Catheter at Home Versus in the Hospital: Obstetric Outcomes and Patient Satisfaction","BALHOME","Inclusion Criteria:\n\n* Medical indication or request for induction\n* Patients between 37 and 41+5 weeks of gestation\n* Singleton pregnancy, cephalic presentation, intact membranes\n* Normal amniotic fluid volume at the time of induction\n* Residing within 30 minutes of the maternity unit and having access to a vehicle\n* Access to a telephone, good understanding of monitoring instructions\n\nExclusion Criteria:\n\n* Scarred uterus\n* Multiple pregnancy\n* Breech presentation\n* Rupture of membranes, hydramnios\n* Placenta previa or low-lying placenta, or significant unexplained bleeding\n* Intrauterine growth restriction, small for gestational age, or known fetal condition requiring fetal monitoring or prompt care at birth\n* Intrauterine fetal death or medical termination of pregnancy\n* Preeclampsia or gestational hypertension\n* Maternal condition requiring hospital monitoring.","FEMALE","18 Years",{"count":74,"type":75},100,"ESTIMATED","6 Days","OBSERVATIONAL","An increasing proportion of patients undergo labor induction at the end of pregnancy. Balloon induction at home is a method validated in the literature.\n\nHome-based balloon induction is already part of routine care at the Paule de Viguier maternity unit. However, a prospective evaluation of this home induction option has not yet been conducted at our facility or elsewhere in France.\n\nOur study will evaluate obstetric outcomes and patient satisfaction regarding this induction method at our center.\n\nThis is an observational, non-interventional, prospective, and comparative-though non-randomized-study.",[80],"Pregnancy",[82,83],"pregnancy","balloon induction","NOT_YET_RECRUITING","2026-09-23",{"date":87,"type":88},"2026-09-30","ACTUAL",{"date":90,"type":75},"2026-11-01",{"date":92,"type":75},"2027-11-06",{"name":5,"class":6},1]