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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05897697
Other study ID # UGeneva 2021-01336
Secondary ID
Status Completed
Phase
First received
Last updated
Start date September 24, 2021
Est. completion date October 7, 2022

Study information

Verified date June 2023
Source University Hospital, Geneva
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

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.


Recruitment information / eligibility

Status Completed
Enrollment 122
Est. completion date October 7, 2022
Est. primary completion date October 7, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria: - women - ongoing pregnancy or within 7 days of delivery - fluency in French or English Exclusion Criteria: - fetal or neonatal death

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Interview
Structured interview

Locations

Country Name City State
France Justine Hugon-Rodin Paris
Switzerland Marc Blondon Geneve

Sponsors (1)

Lead Sponsor Collaborator
Marc Blondon

Countries where clinical trial is conducted

France,  Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Preference for postpartum thromboprophylaxis Risk of postpartum venous thromboembolism at which thromboprophylaxis is preferred 90 days of delivery
Primary Quality-of-life of pulmonary embolism, deep vein thrombosis, postpartum hemorrhage and subcutaneous injections Measurements of utilities of pulmonary embolism, deep vein thrombosis, postpartum hemorrhage and subcutaneous injections, by standard gamble and time trade-off methods 90 days of delivery
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