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Clinical Trial Summary

This non-interventional study will compare the clinical outcomes in women with an event of severe postpartum haemorrhage treated with NovoSeven® to clinical outcomes in women with an event of severe postpartum haemorrhage not treated with NovoSeven®. The study will be a single centre retrospective cohort study of women with an event of severe postpartum haemorrhage, defined as 1.5 L of blood loss within 24 hours of delivery, in the period of 2005-2016.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04444856
Study type Observational
Source Novo Nordisk A/S
Contact
Status Completed
Phase
Start date June 29, 2020
Completion date January 13, 2021

See also
  Status Clinical Trial Phase
Completed NCT01895205 - Treatment of Women After Severe Postpartum Haemorrhage Phase 3