[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Ricardo A Gutierrez Ramirez, MD, MSc, FACOG\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":49},{"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":17,"sex":18,"minAge":19,"maxAge":20,"enrollmentInfo":21,"targetDuration":4,"studyType":24,"phases":25,"briefSummary":27,"conditions":28,"keywords":30,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":48},"100623785","transcutaneous-electrical-nerve-stimulation-tens-for-pain-management-during-labor-100623785",false,"NCT07401147","Transcutaneous Electrical Nerve Stimulation (TENS) for Pain Management During Labor.","Transcutaneous Electrical Stimulation for Pain Reduction During Labor: A Crossover Clinical Trial.","TENS-LABOR","Inclusion Criteria:\n\n* Signed informed consent.\n* Women aged 18-45 years.\n* Nulliparous.\n* Term singleton pregnancy (37-42 weeks).\n* Cephalic presentation.\n* Spontaneous onset of labor or induced\u002Fconducted labor under adequate control.\n* Cervical dilation of at least 5 cm at enrollment.\n* Normal amniotic fluid volume and reassuring fetal monitoring.\n* Uncomplicated pregnancy.\n\nExclusion Criteria:\n\n* Multiple pregnancy.\n* Non-cephalic presentation.\n* Severe obstetric complications (e.g., preeclampsia, placental abruption).\n* Maternal chronic or acute diseases interfering with safety.\n* History of neurological\u002Fpsychiatric disorders contraindicating TENS.\n* Abnormal fetal monitoring or amniotic fluid.\n* Pre-pregnancy BMI \\>30 kg\u002Fm².\n* Fetal demise.\n* Illiteracy.",true,"FEMALE","18 Years","45 Years",{"count":22,"type":23},132,"ESTIMATED","INTERVENTIONAL",[26],"NA","This is a randomized, double-blind, crossover clinical trial to evaluate the efficacy of transcutaneous electrical nerve stimulation (TENS) as a non-pharmacological therapeutic intervention for reducing pain in women during the active phase of labor. Nulliparous women with term pregnancies will be randomly assigned to sequences involving TENS intervention and placebo (device off) periods, separated by a washout. The primary outcome is labor pain intensity measured by the Visual Analog Scale (VAS). Secondary outcomes include duration of the active labor phase, maternal and neonatal safety profile, and childbirth experience satisfaction. The study will be conducted at the Hospital Escuela Universitario from feb 2026 to Ago 2026.",[29],"Labor Pain",[31,32,33,34,35],"labor pain","Transcutaneous Electric Nerve Stimulation","Analgesia","Pain Management","Natural Childbirth","RECRUITING","2026-02-10",{"date":39,"type":40},"2026-02-13","ACTUAL",{"date":42,"type":23},"2026-02-15",{"date":44,"type":23},"2026-09-15",{"name":46,"class":47},"Ricardo A Gutierrez Ramirez, MD, MSc, FACOG","OTHER",2,""]