[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Nicolas Brogly\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":77},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,47],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":22,"conditions":23,"keywords":26,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":46},"100640680","prediction-of-platelet-function-using-viscoelastic-test-rotem-sigma-in-obstetric-anesthesia-100640680",false,"NCT07616349","Prediction of Platelet Function Using Viscoelastic Test (ROTEM® Sigma) in Obstetric Anesthesia.","Prediction of Platelet Function Using Viscoelastic Test (ROTEM® Sigma) in Obstetric Anesthesia: an Prospective Observational Study","Inclusion criteria:\n\n* Parturients with a suspicion or confirmed thrombocytopenia before delivery (platelet count \\\u003C 120x10\\^9\u002FL),\n* Parturients with severe postpartum haemorrhage (blood loss \\>1500 mL) with a suspicion of thrombocytopenia.\n\nExclusion criteria:\n\n* parturient age under 18 years;\n* refusal to participate","FEMALE","18 Years",{"count":19,"type":20},85,"ESTIMATED","OBSERVATIONAL","This prospective observational, non-interventional, single-center study aims to evaluate whether the viscoelastic parameter PLTEM, derived from ROTEM® sigma testing (EXTEM-A5 minus FIBTEM-A5), can accurately estimate platelet count in obstetric patients with thrombocytopenia and\u002For severe postpartum hemorrhage.\n\nThe study will include pregnant women older than 18 years managed during labor and delivery at the Hospital General Universitario Gregorio Marañón, Madrid (Spain).\n\nThe primary objective is to validate the clinical usefulness of PLTEM as a rapid point-of-care tool to support clinical decision-making regarding neuraxial anesthesia and transfusion management in obstetric emergencies.",[24,25],"Thrombocytopenia","Postpartum Haemorrhage (PPH)",[27,28,29,30,31,32,33],"Platelet function","viscoelastic test","Obstetric hemostasis","thrombocytopenia","postpartum haemorrhage","PPH","ROTEM","RECRUITING","2026-05-29",{"date":37,"type":38},"2026-06-01","ACTUAL",{"date":40,"type":38},"2026-05-01",{"date":42,"type":20},"2027-05-01",{"name":44,"class":45},"Nicolas Brogly","OTHER",1,{"id":48,"slug":49,"hasResults":11,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":53,"eligibilityCriteria":54,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":55,"targetDuration":57,"studyType":21,"phases":4,"briefSummary":58,"conditions":59,"keywords":62,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":69,"lastUpdatePostDateStruct":70,"startDateStruct":72,"completionDateStruct":74,"leadSponsor":76,"locationsCount":5},"100629356","failing-epidural-analgesia-during-labor-100629356","NCT07473609","Failing Epidural Analgesia During Labor","Analysis of the Incidence and Risk Factors of Epidural Analgesia Failure During Labor: A Prospective Multicenter Observational Study","FEA25","Inclusion Criteria:\n\n* Parturient who requests epidural analgesia for labor\n\nExclusion Criteria:\n\n* Age under 18 years\n* Stillbirth\n* Continuous spinal anesthesia\n* Refusal to participate",{"count":56,"type":20},500,"2 Days","This prospective multicenter observational study is being conducted at the Gregorio Marañón University General Hospital and the La Paz University Hospital in Madrid, Spain. The recruitment period began on January 12, 2026, and will continue until February 12, 2027. Patients over 18 years of age requesting epidural analgesia for labor are included. Exclusion criteria are: age under 18; stillbirth; continuous spinal anesthesia; refusal to participate in the study. The primary objective of the study is to calculate the incidence of epidural analgesia failure during labor. Secondary objectives are: identification of potential risk factors for epidural analgesia failure; failure of epidural anesthesia for emergency cesarean birth; maternal postpartum recovery at 24 and 48 hours using the Spanish-validated version of ObsQoR-10 questionnaire.",[60,61],"Failed Epidural Analgesia","Post-partum Recovery",[63,64,65,66,67,68],"Labor analgesia","intrapartum cesarean delivery","failed epidural analgesia","breakthrough pain","epidural catheter re-siting","ObsQoR-10","2026-03-12",{"date":71,"type":38},"2026-03-16",{"date":73,"type":38},"2026-01-12",{"date":75,"type":20},"2027-02-12",{"name":44,"class":45},""]