[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"procedural-complication\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:procedural-complication":47},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":4,"hasResults":10,"nctId":11,"briefTitle":12,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":15,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":29,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":5},"100577496",false,"NCT06799052","Cervical Preparation for Same-Day Dilation & Evacuation","Same-Day Cervical Preparation Prior to Second Trimester Dilation & Evacuation: A Noninferiority Randomized Control Trial Comparing Single-Balloon Catheter and Osmotic Dilators","Inclusion Criteria:\n\n* Between 16 weeks 0 days - 18 weeks 6 days gestational age who are pursuing termination, based on reliable gestational age (defined as ultrasonography performed by a clinical provider, or a certain last menstrual period)\n* Able to provide informed consent\n* English- or Spanish-speaking\n* Singleton intrauterine pregnancy\n\nExclusion Criteria:\n\n* Allergy to betadine, aquacryl hydrogel, latex-free silicone single-balloon catheter, synthetic or natural osmotic dilators\n* Fetal demise or known fetal anomaly\n* BMI \\>45\n* Incarceration or other inability to give informed consent\n* Decide to undergo cervical preparation overnight prior to next-day D\\&E",true,"FEMALE","16 Years",{"count":19,"type":20},32,"ESTIMATED","INTERVENTIONAL",[23],"NA","This is a noninferiority randomized control trial of two cervical preparation methods prior to same-day Dilation \\& Evacuation (D\\&E). Cervical preparation is a process that softens and dilates the cervix prior to a procedure.\n\nThe primary objective is to evidence noninferiority of cervical preparation using a single-balloon catheter method when compared to a group receiving osmotic dilators, specifically in D\\&E operative time.\n\nSecondary objectives will compare the two methods for adequate dilation, ability to complete the operation in the same day, participant pain, satisfaction and safety.",[26,27,28],"Abortion, Second Trimester","Procedural Pain","Procedural Complication",[30,31,32,33,34],"Cervical Dilation and Evacuation (D&E)","Transcervical single-balloon catheter","Osmotic dilators","Adequate dilation","Patient satisfaction","RECRUITING","2026-06-29",{"date":38,"type":39},"2026-06-30","ACTUAL",{"date":41,"type":39},"2025-06-12",{"date":43,"type":20},"2026-12",{"name":45,"class":46},"Boston Medical Center","OTHER",""]