[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100593762":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":26,"centralContacts":31,"locations":26,"responsibleParty":37,"collaborators":26,"id":41,"slug":42,"hasResults":43,"nctId":44,"briefTitle":45,"officialTitle":45,"acronym":26,"eligibilityCriteria":46,"healthyVolunteers":47,"sex":48,"minAge":49,"maxAge":50,"enrollmentInfo":51,"targetDuration":26,"studyType":54,"phases":55,"briefSummary":57,"conditions":58,"keywords":26,"overallStatus":60,"whyStopped":26,"lastUpdateSubmitDate":61,"lastUpdatePostDateStruct":62,"startDateStruct":65,"completionDateStruct":67,"leadSponsor":69,"locationsCount":26},{"fullName":5,"class":6},"University of Roma La Sapienza","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Dilapan-S","EXPERIMENTAL","Dilapan-S Participants assigned to the Dilapan-S group will have 3 to 5 rods inserted under aseptic conditions. Placement will follow manufacturer instructions, and rods will remain in place for up to 12 hours unless spontaneous labor or device expulsion occurs earlier. Upon removal, cervical status will be assessed, and induction will continue with prostaglandins or oxytocin based on standard care",[13],"Device: Higroscopic Cervical ripening",{"label":15,"type":16,"description":17,"interventionNames":18},"Double Balloon Catheter (CRB)","ACTIVE_COMPARATOR","Participants randomized to CRB will undergo insertion of a double balloon catheter with inflation of each balloon (approximately 80 mL saline each) according to established protocols. The catheter will remain for up to 12 hours or until spontaneous labor or expulsion. Post-removal management will mirror that of the Dilapan-S group.",[19],"Device: Cervical ripening via CRB",[21,27],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"DEVICE","Higroscopic Cervical ripening","Participants assigned to the Dilapan-S group will have 3 to 5 rods inserted under aseptic conditions. Placement will follow manufacturer instructions, and rods will remain in place for up to 12 hours unless spontaneous labor or device expulsion occurs earlier. Upon removal, cervical status will be assessed, and induction will continue with prostaglandins or oxytocin based on standard care.",[9],null,{"type":22,"name":28,"description":29,"armGroupLabels":30,"otherNames":26},"Cervical ripening via CRB","Double Balloon Catheter (CRB) Participants randomized to CRB will undergo insertion of a double balloon catheter with inflation of each balloon (approximately 80 mL saline each) according to established protocols. The catheter will remain for up to 12 hours or until spontaneous labor or expulsion. Post-removal management will mirror that of the Dilapan-S group.",[15],[32],{"name":33,"role":34,"phone":35,"phoneExt":26,"email":36},"Giuseppe RIZZO, Professor","CONTACT","+393386973001","giuseppe.rizzo@uniroma1.it",{"type":38,"investigatorFullName":39,"investigatorTitle":40,"investigatorAffiliation":5,"oldNameTitle":26,"oldOrganization":26},"PRINCIPAL_INVESTIGATOR","Giuseppe Rizzo","Prof. Giuseppe Rizzo","100593762","dilapan-s-versus-double-balloon-catheter-crb-for-preinduction-of-labor-at-term-100593762",false,"NCT07010653","Dilapan-S Versus Double Balloon Catheter (CRB) for Preinduction of Labor at Term","Inclusion Criteria:\n\n* • Singleton pregnancy\n\n  * Cephalic fetal presentation\n  * Gestational age ≥ 37+0 weeks\n  * Indication for labor induction (e.g., postdates, maternal hypertension)\n  * Bishop score ≤ 6\n  * Maternal age ≥18 years\n  * Ability to provide informed consent\n\nExclusion Criteria:\n\n* • Premature rupture of membranes (PROM)\n\n  * Placenta previa, vasa previa, or abnormal placentation\n  * Active genital tract infection\n  * Prior classical cesarean section or extensive uterine surgery\n  * Known fetal anomaly contraindicating vaginal delivery\n  * Allergy or sensitivity to device materials\n  * Any contraindication to labor induction or vaginal birth",true,"FEMALE","18 Years","45 Years",{"count":52,"type":53},126,"ESTIMATED","INTERVENTIONAL",[56],"NA","Induction of labor (IOL) is a frequently performed procedure in obstetrics, aimed to achieve vaginal delivery when continuing the pregnancy is no longer advisable. A key determinant of IOL success is cervical ripening, particularly when the cervix is initially unfavorable. A range of preinduction methods is available, encompassing both mechanical and pharmacological approaches. Among mechanical techniques, the double balloon catheter (CRB) facilitates cervical dilation by applying direct pressure, which stimulates local prostaglandin release. In contrast, Dilapan-S, a synthetic osmotic dilator, works by gradually expanding through the absorption of cervical fluids, thereby applying gentle mechanical pressure.\n\nWhile both methods are widely used and generally considered safe, there is limited evidence directly comparing their effectiveness and patient-centered outcomes. Mechanical methods are associated with a lower risk of uterine hyperstimulation compared to pharmacological alternatives. The choice between CRB and Dilapan-S may significantly influence labor duration, cesarean delivery rates, maternal comfort, and hospital resource utilization. This study aims to fill the existing knowledge gap by directly comparing Dilapan-S and CRB for term preinduction, with a focus on clinical efficacy and maternal satisfaction.",[59],"Induction of Labor","NOT_YET_RECRUITING","2025-05-29",{"date":63,"type":64},"2025-06-08","ACTUAL",{"date":66,"type":53},"2025-09",{"date":68,"type":53},"2026-12",{"name":5,"class":6}]