Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 3:54 AM
Ignite Modification Date:
2025-12-25 @ 3:54 AM
NCT ID:
NCT06255002
Eligibility Criteria:
Inclusion Criteria:
Adult patients having been informed of the study and not having objected to their participation and treated for severe postpartum haemorrhage defined as bleeding greater than 1000 ml within 24 hours postpartum, whatever the route delivery (vaginal route and caesarean section).
Exclusion Criteria:
* Opposition to participation in the study
* Presence of a constitutional fibrinogen deficiency
* Patients under guardianship or curatorship
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT06255002
Study Brief:
Protocol Section:
NCT06255002