interview
OtherStructured interview
NCT Number: NCT05897697
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.
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Notify Me18 year and older
Female
Observational
Justine Hugon-Rodin, Paris, France
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Structured interview
Time frame: 90 days of delivery
Risk of postpartum venous thromboembolism at which thromboprophylaxis is preferred
Time frame: 90 days of delivery
Measurements of utilities of pulmonary embolism, deep vein thrombosis, postpartum hemorrhage and subcutaneous injections, by standard gamble and time trade-off methods
Marc Blondon
Other
Acronym: PREFER-PP
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