Hemorrhage Clinical Trial
Official title:
Efficacy Study of the Non-Pneumatic Anti-Shock Garment (NASG) in Egypt
This study will test the efficacy of the NASG on women suffering from obstetric hemorrhage as compared to hemorrhaging women who do not receive the NASG.
This is a comparative, pre-post study of the Non-pneumatic Anti-Shock Garment (NASG) to
establish its effectiveness in reducing maternal mortality and morbidity due to obstetrical
hemorrhage. The sites are two maternity teaching hospitals in Egypt: El Galaa, in Cairo and
Assiut University in Assiut.
Our main aim was to test the efficacy of the NASG on women suffering from obstetric
hemorrhage as compared to hemorrhaging women who do not receive the NASG. Our primary
outcome was Extreme Adverse Outcomes (EAO) - a combined outcome of maternal mortality and
severe morbidity. Secondary outcomes included mean measured blood loss and incidence of
emergency hysterectomy.
;
Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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