[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Matild Keresztes\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":43},{"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":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":17,"targetDuration":4,"studyType":20,"phases":21,"briefSummary":23,"conditions":24,"keywords":27,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":5},"100640054","comparative-analysis-of-the-impact-of-transversus-abdominis-plane-block-on-post-cesarean-pain-management-using-low-concentration-ropivacaine-02-100640054",false,"NCT07604376","Comparative Analysis of the Impact of Transversus Abdominis Plane Block on Post-Cesarean Pain Management Using Low Concentration Ropivacaine 0,2%","Inclusion Criteria:\n\npregnant patient anaesthesia type for c-section: spinal\n\nExclusion Criteria:\n\ngeneral anaesthesia for c-section combined spinal\u002Fepidural anaethesia for c-section hipertensive emergencies in obstetrics haemorrhage emergencies in obstetrics","FEMALE","18 Years",{"count":18,"type":19},70,"ESTIMATED","INTERVENTIONAL",[22],"NA","The goal of this clinical trial is to evaluate whether the addition of a Transversus Abdominis Plane (TAP) block improves postoperative outcomes in women undergoing cesarean section.\n\nThe main questions it aims to answer are:\n\nDoes the TAP block reduce postoperative pain scores compared with the traditional analgesic regimen used in our hospital? Does the TAP block decrease opioid consumption within the first 24 hours? Does the TAP block improve the 24-hour quality of recovery? Researchers will compare patients receiving the traditional analgesic regimen with patients who receive the TAP block in addition to standard care to determine differences in pain management, opioid requirements, and recovery quality.\n\nParticipants will:\n\nReceive standard anesthetic and perioperative care for cesarean delivery. Be randomized to either the TAP block group or the traditional analgesic regimen group.\n\nHave postoperative pain scores assessed at predefined intervals. Have opioid consumption recorded within the first 24 hours. Complete a quality-of-recovery assessment at 24 hours postoperatively.",[25,26],"Postoperative Pain","Postoperative Acute Pain",[28,29,30],"obstetric","c-section","TAP block","RECRUITING","2026-05-17",{"date":34,"type":35},"2026-05-22","ACTUAL",{"date":37,"type":35},"2024-03-01",{"date":39,"type":19},"2027-12-31",{"name":41,"class":42},"Matild Keresztes","OTHER",""]