[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100590204":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":11,"centralContacts":11,"locations":27,"responsibleParty":47,"collaborators":11,"id":49,"slug":11,"hasResults":50,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":54,"eligibilityCriteria":55,"healthyVolunteers":50,"sex":56,"minAge":57,"maxAge":11,"enrollmentInfo":58,"targetDuration":11,"studyType":61,"phases":62,"briefSummary":64,"conditions":65,"keywords":11,"overallStatus":29,"whyStopped":11,"lastUpdateSubmitDate":67,"lastUpdatePostDateStruct":68,"startDateStruct":71,"completionDateStruct":73,"leadSponsor":75,"locationsCount":76},{"fullName":5,"class":6},"University of New Mexico","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Cervical Ripening Balloon","EXPERIMENTAL",null,[13],"Device: Cervical Ripening Balloon",{"label":15,"type":16,"description":11,"interventionNames":17},"Osmotic Dilators","ACTIVE_COMPARATOR",[18],"Device: Osmotic Dilators",[20,24],{"type":21,"name":9,"description":22,"armGroupLabels":23,"otherNames":11},"DEVICE","30 milliliter Foley balloon",[9],{"type":21,"name":15,"description":25,"armGroupLabels":26,"otherNames":11},"Dilapan-S",[15],[28],{"facility":5,"status":29,"city":30,"state":31,"zip":32,"country":33,"countryCode":34,"cosmosGeoPoint":35,"geoPoint":40,"contacts":41},"RECRUITING","Albuquerque","New Mexico","87106","United States","US",{"type":36,"coordinates":37},"Point",[38,39],-106.65114,35.08449,{"lat":39,"lon":38},[42],{"name":43,"role":44,"phone":45,"phoneExt":11,"email":46},"Cervical Ripening Balloon Study Coordinator","CONTACT","505-205-4118","HSC-FamilyPlanningResearch@salud.unm.edu",{"type":48,"investigatorFullName":11,"investigatorTitle":11,"investigatorAffiliation":11,"oldNameTitle":11,"oldOrganization":11},"SPONSOR","100590204",false,"NCT06964373","Cervical Ripening Balloons for Same-Day Cervical Prep","Cervical Ripening Balloon for Same-Day Cervical Preparation for Second Trimester Termination","CRB","Inclusion Criteria:\n\n* Individuals who desire outpatient dilation and evacuation (D\\&E)\n* At least 18 years of age\n* Able and willing to consent\n* Gestational duration between 18 weeks 0 days and 19 weeks 6 days as determined by ultrasound\n* Able to read and understand English or Spanish\n* Able to obtain reliable post-procedure transportation\n* Able to observe fasting guidelines of 6 hours prior to the D\\&E procedure\n\nExclusion Criteria:\n\n* Medical conditions that require procedural management in the operating room\n* Preference for D\\&E procedure in the operating room","FEMALE","18 Years",{"count":59,"type":60},70,"ESTIMATED","INTERVENTIONAL",[63],"NA","The goal of this clinical trial is to learn if a cervical ripening balloon (Foley balloon) works to prepare the cervix before same-day outpatient dilation and evacuation (D\\&E). The main questions it aims to answer are:\n\n* Is cervical preparation with cervical ripening balloon for same-day outpatient D\\&E non-inferior to cervical preparation with osmotic dilators?\n* How feasible and safe is cervical preparation with cervical ripening balloon for same-day outpatient D\\&E?\n* How acceptable is cervical preparation with cervical ripening balloon for same-day outpatient D\\&E?\n\nParticipants will:\n\n* Have cervical preparation with cervical ripening balloon (experimental group) or osmotic dilators (usual care group)\n* Complete two surveys, one about the cervical preparation and one about the D\\&E procedure",[66],"Dilation and Evacuation","2026-05-01",{"date":69,"type":70},"2026-05-05","ACTUAL",{"date":72,"type":70},"2025-04-08",{"date":74,"type":60},"2026-07-31",{"name":5,"class":6},1]