[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"membrane-stripping\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:membrane-stripping":32},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,48],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":20,"enrollmentInfo":21,"targetDuration":4,"studyType":24,"phases":25,"briefSummary":27,"conditions":28,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"100561521","membrane-stripping-for-cervical-ripening-100561521",false,"NCT06591247","Membrane Stripping for Cervical Ripening","Evaluation of Stripping for Cervical Ripening - A Randomized Controlled Study","Stripping","Inclusion Criteria:\n\n* Patients aged 18 and above\n* Patients with a cervical dilation of at least 1 cm\n* Full-term pregnancy\n* Cephalic presentation\n* No contraindication to vaginal delivery\n\nExclusion Criteria:\n\n* Patients with rupture of membranes\n* Patients who do not require cervical ripening and proceed directly to the delivery room for induction with oxytocin\n* Patients for whom the use of a double-balloon catheter\u002FPGE2 is contraindicated\n* Twin pregnancies\n* Pregnancies with macrosomic fetuses where vaginal delivery is contraindicated\n* Patients with maternal or fetal pathologies that do not allow for vaginal delivery due to concerns about fetal or maternal distress",true,"FEMALE","18 Years","50 Years",{"count":22,"type":23},400,"ESTIMATED","INTERVENTIONAL",[26],"NA","The goal of this interventional study is to evaluate the effectiveness of membrane stripping in cervical ripening compared to double balloon catheter induction.\n\nThe study population consists of women undergoing labor induction.\n\nThe main questions it aims to answer are:\n\n1. Is membrane stripping as effective as double balloon catheter induction in cervical ripening?\n2. What is the influence of membrane stripping on the time required for cervical ripening, delivery duration, and maternal and fetal outcomes compared to balloon induction.",[29,30,31,32,33,34],"Labor, Induced","Cervical Ripening","Balloon Induction","Membrane Stripping","Pregnancy Related","Induction of Birth","RECRUITING","2026-04-10",{"date":38,"type":39},"2026-04-15","ACTUAL",{"date":41,"type":39},"2024-08-07",{"date":43,"type":23},"2027-12-31",{"name":45,"class":46},"Meir Medical Center","OTHER",1,{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":4,"eligibilityCriteria":54,"healthyVolunteers":11,"sex":18,"minAge":19,"maxAge":55,"enrollmentInfo":56,"targetDuration":4,"studyType":24,"phases":58,"briefSummary":59,"conditions":60,"keywords":62,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":75,"completionDateStruct":77,"leadSponsor":79,"locationsCount":5},"100596256","the-sweep-trial-a-randomized-controlled-trial-100596256","NCT07043088","The SWEEP Trial: a Randomized Controlled Trial","The SWEEP Trial - Serial Versus no Membrane Sweeping on Spontaneous Onset of Labor: a Randomized Controlled Trial","Inclusion Criteria:\n\nSingleton pregnant women at term with a fetus in cephalic presentation and an intended vaginal delivery.\n\nExclusion Criteria:\n\n* \\\u003C 18 years of age\n* Unable to speak and understand Danish\n* Uncertain gestational age , defined as gestational age not determined by Crown-Rump-Length\n* Previous cesarean section\n* Ruptured membranes\n* Painful contractions\n* Vaginal bleeding more than bloody discharge\n* Membrane sweeping performed within the last two weeks\n* Already scheduled IOL or any known indication for IOL at or prior to GA 41+3 based on local or national guidelines\n* Known low-lying placenta (placenta located \\\u003C3 cm from the internal orifice verified by transvaginal ultrasound)","40 Years",{"count":57,"type":23},1536,[26],"The purpose of this clinical trial is to determine whether serial membrane sweeping at term is more effective than no membrane sweeping in promoting spontaneous onset of labor.\n\nThe primary research question is whether serial membrane sweeping increases the likelihood of birth before gestational age 41+3 with spontaneous onset of labor.\n\nA total of 1536 participants will be randomized between gestational age 39+5 and 40+2 to either no membrane sweeping or up to three membrane sweepings performed 2-3 days apart.\n\nResearchers will collect data from the electronic medical record and participants will be asked to complete a short daily questionnaire on pregnancy symptoms and, in the intervention group, their experience of membrane sweeping from randomization until birth. All participants will be asked to complete a follow-up questionnaire about their birth experience five weeks postpartum",[32,30,61],"Memrane Sweeping",[63,64,65,66,67,68,69,70,71],"membrane sweeping","cervical ripening","labor onset","term pregnancy","induction of labor","midwifery","randomized controlled trial","post-term pregnancy","membrane stripping","2025-08-29",{"date":74,"type":39},"2025-09-02",{"date":76,"type":39},"2025-06-18",{"date":78,"type":23},"2027-10",{"name":80,"class":46},"University of Aarhus"]