[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Instituto Materno Infantil Prof. Fernando Figueira\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":69},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,42],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":31,"startDateStruct":34,"completionDateStruct":36,"leadSponsor":38,"locationsCount":41},"100629854","low-level-laser-therapy-in-pain-and-perineal-healing-in-the-immediate-postpartum-period-a-randomized-clinical-trial-100629854",false,"NCT07480083","Low-level Laser Therapy in Pain and Perineal Healing in the Immediate Postpartum Period: a Randomized Clinical Trial.","Effectiveness of Low-Level Laser Therapy Compared to Sham Treatment on Pain Intensity and Perineal Wound Healing Quality in the Immediate Postpartum Period: A Randomized Clinical Trial","LaserPerineal","Inclusion Criteria:\n\nPostpartum women\u002Fmultiparous women aged 18 years or older;\n\nPostpartum women\u002Fmultiparous women in the immediate postpartum period after vaginal birth;\n\nPostpartum women\u002Fmultiparous women with spontaneous perineal laceration (Grade II, III, or IV);\n\nPostpartum women\u002Fmultiparous women with an average pain score of at least 3 on the Visual Analog Scale (VAS);\n\nLabor duration up to 18 hours.\n\nExclusion Criteria:\n\nPostpartum women\u002Fmultiparous women classified as high-risk during pregnancy due to a diagnosis of gestational diabetes mellitus; type 1 or type 2 diabetes mellitus; chronic or pregnancy-specific hypertension; smoking; alcohol use; use of psychoactive substances, among others;\n\nPostpartum women\u002Fmultiparous women who present postpartum complications (such as hemorrhage, difficulty in verbal communication, or sepsis);\n\nPostpartum women\u002Fmultiparous women who develop clinical or hemodynamic complications after childbirth;\n\nPostpartum women\u002Fmultiparous women whose newborns died or were admitted to a Neonatal Intensive Care Unit (NICU);\n\nWomen with communication difficulties (impaired understanding or mental disorders).","FEMALE","18 Years",{"count":20,"type":21},206,"ESTIMATED","INTERVENTIONAL",[24],"NA","This randomized clinical trial aims to evaluate the effectiveness of low-level laser therapy compared with sham treatment on pain intensity and perineal wound healing quality in the immediate postpartum period. The study seeks to determine whether low-level laser therapy can reduce perineal pain and improve healing outcomes in women with perineal trauma after vaginal birth.",[27,28],"Pain","Perineal Healing","NOT_YET_RECRUITING","2026-03-13",{"date":32,"type":33},"2026-03-18","ACTUAL",{"date":35,"type":21},"2026-04-01",{"date":37,"type":21},"2026-11-01",{"name":39,"class":40},"Instituto Materno Infantil Prof. Fernando Figueira","OTHER",1,{"id":43,"slug":44,"hasResults":11,"nctId":45,"briefTitle":46,"officialTitle":47,"acronym":4,"eligibilityCriteria":48,"healthyVolunteers":49,"sex":50,"minAge":18,"maxAge":4,"enrollmentInfo":51,"targetDuration":4,"studyType":22,"phases":53,"briefSummary":54,"conditions":55,"keywords":58,"overallStatus":60,"whyStopped":4,"lastUpdateSubmitDate":61,"lastUpdatePostDateStruct":62,"startDateStruct":64,"completionDateStruct":66,"leadSponsor":68,"locationsCount":41},"100562316","effectiveness-of-a-intraoperative-blood-recovery-system-in-cardiovascular-surgery-in-brazil-100562316","NCT06601582","Effectiveness of a Intraoperative Blood Recovery System in Cardiovascular Surgery in Brazil","Effectiveness of a Intraoperative Blood Recovery System in Cardiovascular Surgery Using Cardiopulmonary Bypass in Brazil. Randomized Crontrolled Trial","Inclusion Criteria:\n\n* all patients undergoing CABG or Valve surgery singly.\n\nExclusion Criteria:\n\n* Emergency cardiac surgery;\n* Previous heart surgery;\n* End-stage chronic kidney disease;\n* Inability to receive a blood transfusion (refusal);\n* Anemia (hemoglobin less than 10g\u002Fdl);\n* Thrombocytopenia (platelet count less than 100,000\u002Fmm3);\n* Coagulopathy (RNI \\> 1.5);",true,"ALL",{"count":52,"type":21},60,[24],"Randomized trial to evaluate the effectiveness of a intra operative blood recovery system in reducing the need for allogeneic transfusion in cardiovascular surgeries using cardiopulmonary bypass",[56,57],"Cardiovascular Surgery","Blood Loss, Surgical",[56,59],"Operative Blood Salvage","RECRUITING","2024-09-15",{"date":63,"type":33},"2024-09-19",{"date":65,"type":33},"2022-04-01",{"date":67,"type":21},"2024-12-31",{"name":39,"class":40},""]