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NCT03449420 Clinical Trial

Predictability of Thromboelastography Parameters in Severe Post Partum Hemorrhage

Post Partum Hemorrhage Clinical Trial

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

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03449420
Other study ID # ArmandTrousseau
Secondary ID
Status Completed
Phase N/A
First received March 30, 2017
Last updated February 27, 2018
Start date January 2012
Est. completion date July 2015

Study information
Verified date February 2018
Source Hôpital Armand Trousseau
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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

Recruitment information / eligibility
Status Completed
Enrollment 100
Est. completion date July 2015
Est. primary completion date July 2015
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Women presenting with a post partum hemorrhage

- needing sulprostone infusion

- during third trimester of pregnancy

Exclusion Criteria:

- known coagulation disorders

Study Design

Related Conditions & MeSH terms

Intervention

Diagnostic Test:
• thromboelastography
TEG5000® : Kaolin and Functional Fibrinogen tests on native blood sample

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Hôpital Armand Trousseau

Outcome
Type Measure Description Time frame Safety issue
Primary Calculated blood loss 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.) during the 24 hours after delivery
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