[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"cervical-preparation\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:cervical-preparation":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":29,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":5},"100554674","phase-1-mifepristone-vs-misoprostol-100554674",false,"NCT06502158","Mifepristone vs Misoprostol","Mifepristone Versus Misoprostol for Cervical Preparation Prior to Procedural Abortion at 12 to 16 Weeks' Gestation in an Academic Medical Center: a Randomized Controlled Pilot Trial","Inclusion Criteria:\n\n* English or Spanish-speaking\n* Capacity to consent\n* Seeking induced abortion of a singleton pregnancy between 12 weeks, 0 days and 16 weeks, 6 days (based on age at day of surgery)\n\nExclusion Criteria:\n\n* History of more than two prior Cesarean deliveries\n* Sonographic evidence of placenta previa\n* Sonographic concern for morbidly adherent placenta\n* Prior obstetric hemorrhage requiring transfusion\n* Obstructive cervical or lower uterine segment fibroid\n* Current therapeutic anticoagulation use\n* Cerclage in situ\n* History of more than one prior cervical excisional procedure\n* BMI greater than 50 kg\u002Fm\\^2",true,"FEMALE","18 Years","45 Years",{"count":21,"type":22},94,"ESTIMATED","INTERVENTIONAL",[25],"PHASE1","The Investigator team hypothesizes that in a randomized trial comparing mifepristone-alone or misoprostol-alone for cervical preparation for procedural abortions at 12 to 16 weeks in hospital-based care, the proportion of patients who achieve successful cervical dilation will be different between the study groups.",[28],"Cervical Preparation",[30,31,32,33],"Procedural Abortion","Surgical Abortion","Abortion, First Trimester","Cervical Dilators","RECRUITING","2026-07-23",{"date":37,"type":38},"2026-07-24","ACTUAL",{"date":40,"type":38},"2024-10-31",{"date":42,"type":22},"2027-06",{"name":44,"class":45},"Montefiore Medical Center","OTHER"]