To establish a clinical registry of suspected cases of AFE. The existing registry will be migrated to a new platform,
All subjects or their next of kin must be able to provide a signed and dated informed consent form.
In the case of lethal AFE, the surviving family member or next of kin must be able to provide a signed and dated informed consent form with an accompanying death certificate and proof of legal kinship.
Participants are expected to be willing to permit collection of data about their affected pregnancy, previous and future pregnancies, and their current and future health conditions.
Providing biological samples is not required for enrollment.
The inability of an individual to provide a signed and dated informed consent form or those who do not wish to participate.
The University of Texas Health Science Center, Houston
Lead sponsor
Amniotic Fluid Embolism (AFE) Foundation
Collaborator