Predictability of Thromboelastography Parameters in Severe Post Partum Hemorrhage

Predictability of Thromboelastography Parameters in Severe Post Partum Hemorrhage : a Retrospective Study

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT03449420

Enrollment

100

Registered

2018-02-28

Start date

2012-01-31

Completion date

2015-07-31

Last updated

2018-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Post Partum Hemorrhage

Keywords

thromboelastography

Brief summary

The aim of the study is to determine if thromboelastography parameters can be predictive of severe post partum hemorrhage.

Interventions

DIAGNOSTIC_TESTthromboelastography

TEG5000® : Kaolin and Functional Fibrinogen tests on native blood sample

Study design

Observational model

COHORT

Time perspective

RETROSPECTIVE

Eligibility

Sex/Gender

FEMALE

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* Women presenting with a post partum hemorrhage * needing sulprostone infusion * during third trimester of pregnancy

Exclusion criteria

* known coagulation disorders

Design outcomes

Primary

Measure	Time frame	Description
Calculated blood loss	during the 24 hours after delivery	Calculated blood loss at 24 hours after delivery (Sum of the volume of blood transfused and the volume of blood loss calculated by the decrease in hematocrit.)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026