Perinatal bleeding
Conditions
Interventions
None listed
Sponsors
Saitama Medical Center, Saitama Medical University
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Parturients must have oral communication ability; can provide written informed consent signed by herself under her free will after receiving full explanation of the study.
Exclusion criteria
Exclusion criteria: Parturients who do not consent to the nature of the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The simulation of the dilution clotting disorder and consumption coagulopathy in obstetrics bleeding is carried out by in vitro using ROTEM. | — |
Countries
Japan
Contacts
Public ContactYoshifumi Suga
Saitama Medical Center, Saitama Medical University Division of Obstetric Anesthesia, Department of Anesthesiology
Outcome results
None listed