[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"labor-stage-first\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:labor-stage-first":46},{"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":14,"eligibilityCriteria":15,"healthyVolunteers":10,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":28,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":5},"100564974",false,"NCT06636149","Maternal Maneuvers During Prolonged Labor","CIRCUIT: Maternal Maneuvers During Prolonged Labor, A Pilot Randomized Control Trial","CIRCUIT","Inclusion Criteria:\n\n* English-speaking patients\n* Singleton, vertex pregnancies\n* 34 weeks' gestation or later\n* Admitted to Labor and Delivery in spontaneous labor or for an induction of labor\n* Prolonged labor course as defined by: cervical dilation less than 6 cm after 8 hours or more of ruptured membranes (spontaneous or artificial) and oxytocin infusion, or cervical dilation 6 cm or more and less than 1-cm cervical dilation change over 2 hours or more with ruptured membranes and oxytocin infusion\n\nExclusion Criteria:\n\n* Intraamniotic infection prior to randomization\n* Magnesium sulfate treatment\n* Major fetal anomalies\n* BMI ≥50\n* Non-reassuring fetal status prior to randomization\n* Any maternal diagnosis that precludes safety or feasibility of intrapartum circuit of maternal position changes","FEMALE","12 Years",{"count":19,"type":20},82,"ESTIMATED","INTERVENTIONAL",[23],"NA","This pilot, randomized control trial will test whether or not a specific circuit of position changes improves maternal outcomes in cases of prolonged labor.\n\nPatient who have prolonged labor will be approached for consent and randomization to one of two study groups: circuit intervention against routine standard of care position changes. 82 patients will be enrolled in the study. Exclusion criteria will include: any uterine infection prior to randomization, magnesium sulfate treatment, major fetal anomalies, BMI ≥50, non-reassuring fetal status prior to randomization, or any maternal diagnosis that precludes safety or feasibility of the circuit of maternal position changes.\n\nThe 3 aims of the study will include: the outcome that the circuit of position changes has on the duration of the first stage of labor, maternal and neonatal morbidity, and maternal satisfaction.",[26,27],"Labor Stage, First","Prolonged Labor",[29,30,31,32,33],"Circuit","Position changes","Labor","Prolonged labor","Labor dystocia","RECRUITING","2026-03-11",{"date":37,"type":38},"2026-03-13","ACTUAL",{"date":40,"type":38},"2024-12-10",{"date":42,"type":20},"2028-05-31",{"name":44,"class":45},"Washington University School of Medicine","OTHER",""]