[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Central Clinical Hospital of the Ministry of Internal Affairs and Administration, Warsaw, Poland\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":45},{"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":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":23,"conditions":24,"keywords":28,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":5},"100582249","epidurals-impact-on-contractions-and-fetal-response-100582249",false,"NCT06860854","EPidural's Impact on Contractions and Fetal REsponse","The Effect of Epidural Analgesia on Uterine Contractility and Intrapartum Fetal Well-being - Study Protocol for a Prospective Observational Study \"EPI-CARE\"","EPI-CARE","Inclusion Criteria:\n\n* ≥ 18 years old\n* singleton pregnancy\n* signed informed consent form\n* patients in labor\n* cervical dilation ≥ 3cm,\n* patient requesting and eligible for epidural analgesia\n* normal CTG trace for at least 30 minutes before epidural analgesia\n\nExclusion Criteria:\n\n* \\\u003C than 18 years old\n* preterm delivery\n* labor induced or stimulated by oxytocin\n* multiple pregnancy\n* fetal malformations\n* \\\u003C than 3cm cervical dilation\n* lack of CTG trace for at least 30 minutes before epidural analgesia\n* patient not requesting or not eligible for epidural analgesia\n* informed consent form not signed","FEMALE","18 Years",{"count":20,"type":21},200,"ESTIMATED","OBSERVATIONAL","This prospective observational study aims to assess the impact of epidural analgesia (ELA) on uterine contractility, cardiotocography (CTG) patterns, and maternal-fetal hemodynamics in term pregnancies. The study will recruit 200 laboring patient receiving ELA and evaluate changes in uterine contractions, Doppler blood flow parameters, and fetal heart rate tracings before and after ELA administration. Secondary analyses will compare outcomes between primiparous and multiparous women, as well as between uncomplicated and complicated pregnancies. Pain relief effectiveness will be correlated with observed changes. This study will provide a comprehensive understanding of ELA's effects on labor progression and fetal well-being, addressing gaps in existing research.",[25,26,27],"Epidural Anesthesia in Labor and Delivery","Doppler Ultrasound","Uterine Contraction",[29,30,31,32],"Epidural Analgesia","Uterine Contractility","Maternal-Fetal Hemodynamics","Cardiotocography (CTG) Patterns","NOT_YET_RECRUITING","2025-02-28",{"date":36,"type":37},"2025-03-06","ACTUAL",{"date":39,"type":21},"2025-03-17",{"date":41,"type":21},"2025-12-31",{"name":43,"class":44},"Central Clinical Hospital of the Ministry of Internal Affairs and Administration, Warsaw, Poland","OTHER",""]