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Assessing Women's Preferences for Postpartum Thromboprophylaxis: the Prefer-Postpartum Study

NCT05897697 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 122

Last updated 2023-06-12

No results posted yet for this study

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.

Conditions

  • Venous Thromboembolism
  • Pregnancy Related

Interventions

OTHER

Interview

Structured interview

Sponsors & Collaborators

  • Marc Blondon

    lead OTHER

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-09-24
Primary Completion
2022-10-07
Completion
2022-10-07

Countries

  • France
  • Switzerland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05897697 on ClinicalTrials.gov