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Clinical Trial Summary

The preferences of pregnant women for postpartum thromboprophylaxis are largely unknown. The aims of this transversal study are to elicit the preferences of pregnant/postpartum women about postpartum thromboprophylaxis in semi-structured interviews, and to estimate the utility of the relevant health states (pulmonary embolism, deep vein thrombosis, postpartum hemorrhage, subcutaneous injections). In this second aim, the investigators will also compare the effect of 2 different techniques to estimate utilities (standard gamble vs. time trade-off), using a randomization of these techniques.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05897697
Study type Observational
Source University Hospital, Geneva
Contact
Status Completed
Phase
Start date September 24, 2021
Completion date October 7, 2022

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