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Clinical Trial Summary

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.

Clinical Trial Description


Study Design

Related Conditions & MeSH terms

NCT number NCT05191251
Study type Observational
Source Brugmann University Hospital
Contact Denis Schmartz, MD
Phone +3224773996
Email [email protected]
Status Not yet recruiting
Start date January 20, 2022
Completion date March 31, 2022

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