[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100590204":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":11,"centralContacts":11,"locations":27,"responsibleParty":46,"collaborators":11,"id":48,"slug":11,"hasResults":49,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":53,"eligibilityCriteria":54,"healthyVolunteers":49,"sex":55,"minAge":56,"maxAge":11,"enrollmentInfo":57,"targetDuration":11,"studyType":60,"phases":61,"briefSummary":63,"conditions":64,"keywords":11,"overallStatus":29,"whyStopped":11,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":67,"startDateStruct":70,"completionDateStruct":72,"leadSponsor":74,"locationsCount":75},{"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,"cosmosGeoPoint":34,"geoPoint":39,"contacts":40},"RECRUITING","Albuquerque","New Mexico","87106","United States",{"type":35,"coordinates":36},"Point",[37,38],-106.65114,35.08449,{"lat":38,"lon":37},[41],{"name":42,"role":43,"phone":44,"phoneExt":11,"email":45},"Cervical Ripening Balloon Study Coordinator","CONTACT","505-205-4118","HSC-FamilyPlanningResearch@salud.unm.edu",{"type":47,"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":58,"type":59},70,"ESTIMATED","INTERVENTIONAL",[62],"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",[65],"Dilation and Evacuation","2026-05-01",{"date":68,"type":69},"2026-05-05","ACTUAL",{"date":71,"type":69},"2025-04-08",{"date":73,"type":59},"2026-07-31",{"name":5,"class":6},1]