[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100656720":3},{"organization":4,"outcomesModule":7,"designInfo":42,"detailedDescription":48,"studyPopulation":41,"armGroups":49,"interventions":62,"overallOfficials":71,"centralContacts":76,"locations":41,"responsibleParty":82,"collaborators":41,"id":86,"slug":87,"hasResults":88,"nctId":89,"briefTitle":90,"officialTitle":91,"acronym":41,"eligibilityCriteria":92,"healthyVolunteers":88,"sex":93,"minAge":94,"maxAge":95,"enrollmentInfo":96,"targetDuration":41,"studyType":99,"phases":100,"briefSummary":102,"conditions":103,"keywords":105,"overallStatus":111,"whyStopped":41,"lastUpdateSubmitDate":112,"lastUpdatePostDateStruct":113,"startDateStruct":116,"completionDateStruct":118,"leadSponsor":120,"locationsCount":41},{"fullName":5,"class":6},"Assiut University","OTHER",{"primaryOutcomes":8,"secondaryOutcomes":13,"otherOutcomes":41},[9],{"measure":10,"description":11,"timeFrame":12},"Length of hospital stay","Duration of hospital stay measured in hours from end of cesarean delivery to hospital discharge","Up to 7 days",[14,18,21,25,29,32,35,38],{"measure":15,"description":16,"timeFrame":17},"Postoperative pain score at 6 hours","Pain score assessed using 0 to 10 Visual Analogue Scale with 0 indicating no pain and 10 indicating worst imaginable pain with higher scores indicating worse pain","At 6 hours after surgery",{"measure":19,"description":16,"timeFrame":20},"Postoperative pain score at 24 hours","At 24 hours after surgery",{"measure":22,"description":23,"timeFrame":24},"Time to first ambulation","Time in hours from end of surgery to first ambulation","Up to 48 hours",{"measure":26,"description":27,"timeFrame":28},"Time to first oral intake","Time in hours from end of surgery to first oral fluid intake","Up to 24 hours",{"measure":30,"description":31,"timeFrame":24},"Time to urinary catheter removal","Time in hours from end of surgery to Foley catheter removal",{"measure":33,"description":34,"timeFrame":28},"Postpartum hemorrhage","Number of participants who develop postpartum hemorrhage with blood loss greater than 1000 milliliters",{"measure":36,"description":37,"timeFrame":12},"Requirement for blood transfusion","Number of participants who require packed red blood cells transfusion",{"measure":39,"description":40,"timeFrame":20},"Patient satisfaction score","Score on the Quality of Recovery-15 questionnaire scale ranges from 0 to 150 with higher scores indicating better recovery and satisfaction",null,{"allocation":43,"interventionModel":44,"interventionModelDescription":41,"primaryPurpose":45,"observationalModel":41,"timePerspective":41,"maskingInfo":46},"RANDOMIZED","PARALLEL","SUPPORTIVE_CARE",{"masking":47,"maskingDescription":41,"whoMasked":41},"NONE","Placenta previa is associated with significant maternal morbidity and prolonged hospitalization. Enhanced Recovery After Surgery pathways include patient education preoperative fasting optimization multimodal analgesia early oral intake early mobilization and early urinary catheter removal. This prospective study will include women with singleton pregnancy and sonographic diagnosis of placenta previa scheduled for elective cesarean delivery at Assiut University Hospital. Group A will receive ERAS pathway and Group B will receive conventional care. Outcomes including length of hospital stay postoperative pain time to ambulation time to oral intake and patient satisfaction will be compared.",[50,56],{"label":51,"type":52,"description":53,"interventionNames":54},"ERAS Group","EXPERIMENTAL","Women managed according to the standardized ERAS pathway including preoperative education fasting 2 hours for clear fluids multimodal analgesia early oral intake early mobilization and early urinary catheter removal",[55],"Other: Enhanced Recovery After Surgery Protocol",{"label":57,"type":58,"description":59,"interventionNames":60},"Conventional Care Group","ACTIVE_COMPARATOR","Women managed with routine perioperative care currently practiced in the department",[61],"Other: Conventional perioperative care",[63,67],{"type":6,"name":64,"description":65,"armGroupLabels":66,"otherNames":41},"Enhanced Recovery After Surgery Protocol","Standardized ERAS pathway for cesarean delivery including preoperative counseling, clear fluids allowed up to 2 hours and solid food fasting for 6 hours, optimization of hemoglobin, multimodal analgesia with scheduled acetaminophen and nonsteroidal anti-inflammatory drugs with limited opioids, prophylaxis for postoperative nausea and vomiting, early oral fluid and solid intake, early mobilization with sitting and standing and ambulation within 6 to 12 hours, early Foley catheter removal within 12 hours when clinically feasible, and standardized discharge planning. This intervention is applied only to the Experimental Arm.",[51],{"type":6,"name":68,"description":69,"armGroupLabels":70,"otherNames":41},"Conventional perioperative care","Routine conventional perioperative care currently practiced at Assiut University Hospital including traditional preoperative fasting, standard analgesia, usual timing of oral intake, mobilization and urinary catheter removal according to physician preference.",[57],[72],{"name":73,"affiliation":74,"role":75},"Ahmed A Abdel-Aleem, prof","Department of Obstetrics and Gynecology Assiut University Hospital Assiut Egypt","STUDY_CHAIR",[77],{"name":78,"role":79,"phone":80,"phoneExt":41,"email":81},"Ahmed M Adly, Resident","CONTACT","01015727207","Ahmed.18313583@med.aun.edu.eg",{"type":83,"investigatorFullName":84,"investigatorTitle":85,"investigatorAffiliation":5,"oldNameTitle":41,"oldOrganization":41},"PRINCIPAL_INVESTIGATOR","Ahmed Mostafa Adly Embaby","Resident Physician, Obstetrics and Gynecology department","100656720","eras-protocol-for-cesarean-delivery-in-women-with-placenta-previa-100656720",false,"NCT07830914","ERAS Protocol for Cesarean Delivery in Women With Placenta Previa","Impact of Enhanced Recovery After Surgery Protocol on Maternal Recovery Patient Satisfaction and Length of Hospital Stay Following Cesarean Delivery in Women With Placenta Previa","Inclusion Criteria:\n\n* Singleton pregnancy\n* Sonographic diagnosis of placenta previa\n* Scheduled for elective cesarean delivery\n* Ability to provide informed consent\n\nExclusion Criteria:\n\n* Severe medical diseases affecting postoperative recovery including hypertension and diabetes mellitus\n* Hemodynamic instability before surgery\n* ICU admission immediately after surgery\n* Refusal to participate","FEMALE","18 Years","45 Years",{"count":97,"type":98},100,"ESTIMATED","INTERVENTIONAL",[101],"NA","This study aims to evaluate the impact of Enhanced Recovery After Surgery protocols on maternal outcomes patient satisfaction and length of hospital stay following cesarean delivery in women with placenta previa. Women scheduled for elective cesarean delivery for placenta previa will be managed either with a standardized ERAS pathway or with conventional routine perioperative care.",[104],"Placenta Previa",[106,107,108,104,109,110],"Patient satisfaction","ERAS","Enhanced Recovery","Length of stay","Assiut","NOT_YET_RECRUITING","2026-09-18",{"date":114,"type":115},"2026-09-22","ACTUAL",{"date":117,"type":98},"2026-09-20",{"date":119,"type":98},"2028-03-10",{"name":5,"class":6}]