[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100598922":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":18,"centralContacts":25,"locations":31,"responsibleParty":43,"collaborators":18,"id":46,"slug":47,"hasResults":48,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":18,"eligibilityCriteria":52,"healthyVolunteers":48,"sex":53,"minAge":54,"maxAge":18,"enrollmentInfo":55,"targetDuration":18,"studyType":58,"phases":59,"briefSummary":61,"conditions":62,"keywords":64,"overallStatus":68,"whyStopped":18,"lastUpdateSubmitDate":69,"lastUpdatePostDateStruct":70,"startDateStruct":73,"completionDateStruct":75,"leadSponsor":77,"locationsCount":78},{"fullName":5,"class":6},"Adiyaman University Research Hospital","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Epidural group- group E","EXPERIMENTAL","Participants in this group will receive epidural analgesia during vaginal delivery",[13],"Procedure: Epidural Analgesia",{"label":15,"type":16,"description":17,"interventionNames":18},"Control group- group C","NO_INTERVENTION","Participants in this group will undergo vaginal delivery without receiving any form of neuraxial analgesia.",null,[20],{"type":21,"name":22,"description":23,"armGroupLabels":24,"otherNames":18},"PROCEDURE","Epidural Analgesia","After informed consent and exclusion of contraindications, an epidural catheter will be placed at the L3-L4 interspace in the sitting position using a Tuohy needle. A test dose of 2 mL lidocaine will be administered to confirm correct catheter placement under continuous monitoring of vital signs. Once cervical dilatation reaches 5 cm, 5 mL of 0.2% bupivacaine combined with 25 mcg fentanyl will be administered via the epidural catheter. Additional boluses will be given as needed based on pain assessment. The catheter will be removed 24 hours postpartum.",[9],[26],{"name":27,"role":28,"phone":29,"phoneExt":18,"email":30},"Nezir Yılmaz","CONTACT","+905068939496","yilmaznezirr@gmail.com",[32],{"facility":33,"status":18,"city":34,"state":18,"zip":35,"country":36,"countryCode":18,"cosmosGeoPoint":37,"geoPoint":42,"contacts":18},"Adıyaman University Training and Research Hospital","Adıyaman","02200","Turkey (Türkiye)",{"type":38,"coordinates":39},"Point",[40,41],38.27629,37.76441,{"lat":41,"lon":40},{"type":44,"investigatorFullName":27,"investigatorTitle":45,"investigatorAffiliation":5,"oldNameTitle":18,"oldOrganization":18},"PRINCIPAL_INVESTIGATOR","Assoc. Prof.","100598922","the-effects-of-epidural-analgesia-on-maternal-infant-bonding-and-birth-related-trauma-100598922",false,"NCT07077785","The Effects of Epidural Analgesia on Maternal-Infant Bonding and Birth-Related Trauma","The Effects of Epidural Analgesia on Maternal-Infant Bonding and Birth-Related Trauma in Women Undergoing Vaginal Delivery With Epidural Analgesia","Inclusion Criteria:\n\nFemale participants aged between 18 and 40 years\n\nASA physical status classification I or II\n\nPregnant women undergoing spontaneous vaginal delivery at the study hospital\n\nWillingness to provide informed consent and participate in study procedures\n\nExclusion Criteria:\n\nAge below 18\n\nASA physical status classification III or IV\n\nMorbid obesity (BMI ≥ 40 kg\u002Fm²)\n\nIndication for cesarean section\n\nHistory of local anesthetic toxicity or allergy\n\nContraindications to epidural analgesia (e.g., coagulopathy, infection at insertion site)\n\nAny significant maternal or fetal complication that contraindicates study participation","FEMALE","18 Years",{"count":56,"type":57},80,"ESTIMATED","INTERVENTIONAL",[60],"NA","This prospective, single-center study aims to evaluate the effects of epidural analgesia on maternal-infant bonding and perceived birth-related trauma in women undergoing vaginal delivery. Participants will be divided into two groups: those who receive epidural analgesia and those who deliver without it. Standardized questionnaires will be used to assess pain perception, maternal satisfaction, and the quality of early bonding between mother and infant. The study is designed in accordance with the Declaration of Helsinki and Good Clinical Practice guidelines, with approval from the local ethics committee.",[63],"Epidural Anesthesia in Labor and Delivery",[65,66,67],"epidural analgesia","maternal-infant bonding","Psychological Birth Trauma","NOT_YET_RECRUITING","2025-07-12",{"date":71,"type":72},"2025-07-22","ACTUAL",{"date":74,"type":57},"2025-07-25",{"date":76,"type":57},"2025-09-15",{"name":5,"class":6},1]