[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100647195":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":25,"centralContacts":29,"locations":38,"responsibleParty":61,"collaborators":18,"id":64,"slug":65,"hasResults":66,"nctId":67,"briefTitle":68,"officialTitle":69,"acronym":18,"eligibilityCriteria":70,"healthyVolunteers":71,"sex":72,"minAge":73,"maxAge":18,"enrollmentInfo":74,"targetDuration":18,"studyType":77,"phases":78,"briefSummary":80,"conditions":81,"keywords":83,"overallStatus":41,"whyStopped":18,"lastUpdateSubmitDate":87,"lastUpdatePostDateStruct":88,"startDateStruct":91,"completionDateStruct":92,"leadSponsor":94,"locationsCount":95},{"fullName":5,"class":6},"Holy Family Hospital, Nazareth, Israel","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"TENS Group","EXPERIMENTAL","This arm is receiving the active clinical intervention being evaluated in the study (the TENS device). Pain scores will be assessed during two consecutive breastfeeding sessions. The first with, and the second without TENS.",[13],"Device: Transcutaneous Electrical Nerve Stimulation (TENS)",{"label":15,"type":16,"description":17,"interventionNames":18},"No-TENS Control Group","NO_INTERVENTION","Participants assigned to this control group will receive standard postpartum care only, without any TENS application. Pain scores will be assessed during two consecutive breastfeeding sessions within the first 48 hours postpartum to serve as a comparative baseline against the intervention group.",null,[20],{"type":21,"name":22,"description":23,"armGroupLabels":24,"otherNames":18},"DEVICE","Transcutaneous Electrical Nerve Stimulation (TENS)","Bilateral application of four skin electrodes using conductive gel. Two electrodes will be placed on the lower abdomen over the uterus, and two will be placed in parallel in the S2-S4 sacral region. The digital sensory-motor TENS device will be programmed to generate a 100-Hz current and 75 msec pulse for 40 min, using 20-60 mA of intensity. Stimulation begins a few minutes before breastfeeding and continues throughout the 40-minute session.",[9],[26],{"name":27,"affiliation":5,"role":28},"Raed Salim, M.D.","STUDY_CHAIR",[30,35],{"name":31,"role":32,"phone":33,"phoneExt":18,"email":34},"Marwa Bayatra, MD","CONTACT","97246508900","bayatra7@gmail.com",{"name":36,"role":32,"phone":33,"phoneExt":18,"email":37},"RAED SALIM, PROF","r.salim@hfhosp.org",[39,54],{"facility":40,"status":41,"city":42,"state":18,"zip":18,"country":43,"countryCode":44,"cosmosGeoPoint":45,"geoPoint":50,"contacts":51},"Holy Family Hospital","RECRUITING","Nazareth","Israel","IL",{"type":46,"coordinates":47},"Point",[48,49],35.29719,32.70087,{"lat":49,"lon":48},[52],{"name":53,"role":32,"phone":18,"phoneExt":18,"email":37},"Raed Salim, MD",{"facility":40,"status":41,"city":42,"state":18,"zip":18,"country":43,"countryCode":44,"cosmosGeoPoint":55,"geoPoint":57,"contacts":58},{"type":46,"coordinates":56},[48,49],{"lat":49,"lon":48},[59],{"name":60,"role":32,"phone":18,"phoneExt":18,"email":37},"Raed",{"type":62,"investigatorFullName":53,"investigatorTitle":63,"investigatorAffiliation":5,"oldNameTitle":18,"oldOrganization":18},"PRINCIPAL_INVESTIGATOR","PROFESSOR","100647195","tens-for-postpartum-uterine-pain-during-breastfeeding-100647195",false,"NCT07703917","TENS for Postpartum Uterine Pain During Breastfeeding","Transcutaneous Electrical Nerve Stimulation for Treating Postpartum Uterine Pain During Breastfeeding in Multiparous Women: a Randomized Controlled Trial","Inclusion Criteria:\n\n* Maternal Age above 18\n* Term delivery (37 weeks or more)\n* Vaginal delivery within the past 48 hours.\n* Multiparous women (2 or more previous births)\n* Delivery of a singleton\n* Have the well to breastfeed\n\nExclusion Criteria:\n\n* Contraindication to TENS (pacemaker, epilepsy, active infection, uncontrolled hyper \u002F hypotension.)\n* Chronic analgesia use\n* Severe complications requiring intervention (severe PPH) or intensive care\n* Skin lesions, infections, or scars at proposed electrode sites\n* Neonatal intensive care unit admission",true,"FEMALE","18 Years",{"count":75,"type":76},124,"ESTIMATED","INTERVENTIONAL",[79],"NA","This clinical study is designed to evaluate whether Transcutaneous Electrical Nerve Stimulation (TENS) is an effective, non-drug method to relieve postpartum uterine pain during breastfeeding in multiparous women (women who have given birth multiple times). Breastfeeding in the first 48 hours after delivery often triggers strong, painful uterine contractions due to the natural release of oxytocin. While standard care typically relies on pain-relief medications, this study investigates if TENS, a safe, low-cost device that sends gentle electrical impulses through small skin patches, can significantly reduce this pain and decrease the need for systemic medications. Participants will be randomly assigned to either receive standard postpartum pain medications or use a TENS device during two consecutive breastfeeding sessions. Researchers will measure and compare the peak pain levels between both groups using a standard 0 to 10 pain scale. The aim is examining whether TENS will significantly reduce postpartum uterine pain during breastfeeding and decrease medication use compared with standard care.",[82],"Breast Feeding",[84,85,86],"BREASTFEEDING","TENS","POSTPARTUM PAIN","2026-08-15",{"date":89,"type":90},"2026-08-18","ACTUAL",{"date":87,"type":90},{"date":93,"type":76},"2027-08-01",{"name":5,"class":6},2]