[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100453954":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":10,"centralContacts":10,"locations":20,"responsibleParty":33,"collaborators":10,"id":37,"slug":38,"hasResults":39,"nctId":40,"briefTitle":41,"officialTitle":41,"acronym":10,"eligibilityCriteria":42,"healthyVolunteers":39,"sex":43,"minAge":44,"maxAge":10,"enrollmentInfo":45,"targetDuration":10,"studyType":48,"phases":10,"briefSummary":49,"conditions":50,"keywords":10,"overallStatus":54,"whyStopped":10,"lastUpdateSubmitDate":55,"lastUpdatePostDateStruct":56,"startDateStruct":58,"completionDateStruct":60,"leadSponsor":62,"locationsCount":63},{"fullName":5,"class":6},"Brugmann University Hospital","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Full-term pregnant women with HEMSTOP",null,"Full-term pregnant women who have given birth vaginally or by cesarean section. Patients for whom a HEMSTOP questionnaire could be carried out in prepartum, during the pre-delivery anesthesia consultation.\n\nPatients who received follow-up during pregnancy as recommended. Age over 18",[13],"Diagnostic Test: HEMSTOP questionnaire",[15],{"type":16,"name":17,"description":18,"armGroupLabels":19,"otherNames":10},"DIAGNOSTIC_TEST","HEMSTOP questionnaire","A HEMSTOP questionnaire is obtained during the anesthesia consultation.",[9],[21],{"facility":22,"status":10,"city":23,"state":10,"zip":24,"country":25,"countryCode":26,"cosmosGeoPoint":27,"geoPoint":32,"contacts":10},"CHU Brugmann","Brussels","1020","Belgium","BE",{"type":28,"coordinates":29},"Point",[30,31],4.34878,50.85045,{"lat":31,"lon":30},{"type":34,"investigatorFullName":35,"investigatorTitle":36,"investigatorAffiliation":5,"oldNameTitle":10,"oldOrganization":10},"PRINCIPAL_INVESTIGATOR","Denis SCHMARTZ","Head, department of Anesthesiology","100453954","retrospective-assessment-of-the-risk-of-peripartum-hemorrhage-in-pregnant-women--retrospective-assessment-of-the-diagnostic-performance-of-the-hemstop-standardized-questionnaire-100453954",false,"NCT05191251","Retrospective Assessment of the Risk of Peripartum Hemorrhage in Pregnant Women : Retrospective Assessment of the Diagnostic Performance of the HEMSTOP Standardized Questionnaire","Inclusion Criteria:\n\nFull-term pregnant women who have given birth vaginally or by cesarean section. Patients for whom a HEMSTOP questionnaire could be carried out in prepartum, during the pre-delivery anesthesia consultation.\n\nPatients who received follow-up during pregnancy as recommended. Age over 18\n\nExclusion Criteria:\n\nPatients age under the age of 18 Patients who did not have follow-up during pregnancy as recommended Patients taking long-term anticoagulants and\u002For antiaggregants Patients with a language barrier","FEMALE","18 Years",{"count":46,"type":47},3588,"ACTUAL","OBSERVATIONAL","The diagnostic performance of the HEMSTOP (Hematoma, hEmorrhage, Menorrhagia, Surgery, Tooth extraction, Obstetrics, Parents) standardized questionnaire collected during the preoperative anesthesia consultation in order to detect a deficit in hemostasis associated with the risk of hemorrhage in pregnant women will be analyzed. The primary aim of the study is to assess the sensitivity and the specificity of the HEMSTOP questionnaire to identity patients with an abnormal first-line hemostasis test requiring further development by performing second-line hemostasis tests. The second aim of the study is to assess the sensitivity and specificity of the HEMSTOP questionnaire in predicting postpartum hemorrhage.",[51,52,53],"Peripartum Period","Hemorrhage","HEMSTOP Questionnaire","COMPLETED","2022-07-19",{"date":57,"type":47},"2022-07-20",{"date":59,"type":47},"2022-01-13",{"date":61,"type":47},"2022-06-30",{"name":5,"class":6},1]