[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"chronic-post-episiotomy-pain\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:chronic-post-episiotomy-pain":28},{"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":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":30,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":4},"100655331","repeated-pudendal-nerve-block-and-physiotherapy-for-prevention-of-chronic-post-episiotomy-pain-100655331",false,"NCT07814183","Repeated Pudendal Nerve Block and Physiotherapy for Prevention of Chronic Post-Episiotomy Pain","Efficacy of Repeated Pudendal Nerve Block Combined With Physiotherapy for the Prevention of Chronic Post-Episiotomy Pain and Dyspareunia: A Randomized Controlled Trial","REPP","Inclusion Criteria:\n\nParticipants must meet all of the following:\n\n* Women aged 18-40 years.\n* Term pregnancy.\n* Vaginal delivery with episiotomy or first-time perineal tear.\n* Postpartum pain score \\>3\u002F10 within 24 hours after delivery.\n* Willingness to participate and provide informed consent. -\n\nExclusion Criteria:\n\n* Refusal to participate.\n* Previous episiotomy or perineal tear.\n* Pain score ≤3\u002F10.\n* Known allergy to study medications.\n* Pre-existing pudendal neuralgia.\n* Pre-existing dyspareunia.","FEMALE","18 Years","40 Years",{"count":21,"type":22},104,"ESTIMATED","INTERVENTIONAL",[25],"NA","This prospective, single-center, open-label, randomized controlled trial will evaluate whether repeated ultrasound-guided pudendal nerve block combined with standardized physiotherapy and standard postpartum analgesic management reduces persistent post-episiotomy pain and postpartum dyspareunia compared with standard management alone. Women aged 18-40 years who have undergone vaginal delivery with episiotomy or a first-time perineal tear and who report postpartum pain greater than 3\u002F10 within 24 hours after delivery will be randomized in a 1:1 ratio. The intervention group will receive standard management plus a repeated pudendal nerve block before hospital discharge and a second block on postpartum Day 10 if pain remains greater than 3\u002F10. Pain and sexual function will be assessed through 3 months postpartum.",[28,29],"Chronic Post-episiotomy Pain","Postpartum Dyspareunia",[31,32,33,34],"Episiotomy","analgesic pudendal nerve block","Chronic post episiotomy pain","post partum dyspareunia","NOT_YET_RECRUITING","2026-09-07",{"date":38,"type":39},"2026-09-10","ACTUAL",{"date":41,"type":22},"2026-09-01",{"date":43,"type":22},"2027-11-01",{"name":45,"class":46},"Vinmec Healthcare System","OTHER"]