[{"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:":67},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,41],{"id":9,"slug":4,"hasResults":10,"nctId":11,"briefTitle":12,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":10,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":29,"lastUpdatePostDateStruct":30,"startDateStruct":33,"completionDateStruct":35,"leadSponsor":37,"locationsCount":40},"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":19,"type":20},206,"ESTIMATED","INTERVENTIONAL",[23],"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.",[26,27],"Pain","Perineal Healing","NOT_YET_RECRUITING","2026-03-13",{"date":31,"type":32},"2026-03-18","ACTUAL",{"date":34,"type":20},"2026-04-01",{"date":36,"type":20},"2026-11-01",{"name":38,"class":39},"Instituto Materno Infantil Prof. Fernando Figueira","OTHER",1,{"id":42,"slug":4,"hasResults":10,"nctId":43,"briefTitle":44,"officialTitle":45,"acronym":4,"eligibilityCriteria":46,"healthyVolunteers":47,"sex":48,"minAge":17,"maxAge":4,"enrollmentInfo":49,"targetDuration":4,"studyType":21,"phases":51,"briefSummary":52,"conditions":53,"keywords":56,"overallStatus":58,"whyStopped":4,"lastUpdateSubmitDate":59,"lastUpdatePostDateStruct":60,"startDateStruct":62,"completionDateStruct":64,"leadSponsor":66,"locationsCount":40},"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":50,"type":20},60,[23],"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",[54,55],"Cardiovascular Surgery","Blood Loss, Surgical",[54,57],"Operative Blood Salvage","RECRUITING","2024-09-15",{"date":61,"type":32},"2024-09-19",{"date":63,"type":32},"2022-04-01",{"date":65,"type":20},"2024-12-31",{"name":38,"class":39},""]