Predictability of Thromboelastography Parameters in Severe Post Partum Hemorrhage

NCT ID: NCT03449420

Last Updated: 2018-02-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

100 participants

Study Classification

OBSERVATIONAL

Study Start Date

2012-01-31

Study Completion Date

2015-07-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Post Partum Hemorrhage

Keywords

Explore important study keywords that can help with search, categorization, and topic discovery.

thromboelastography

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Post Partum Hemorrhage

Patients presenting with a post partum hemorrhage. A thromboelastography analysis is realized at discretion of the anesthesiologist in charge

thromboelastography

Intervention Type DIAGNOSTIC_TEST

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

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

thromboelastography

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

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

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

Exclusion Criteria

* known coagulation disorders
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Hôpital Armand Trousseau

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Pr Isabelle CONSTANT

Head of Anesthesiology Department

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Agnes Rigouzzo, MD

Role: STUDY_DIRECTOR

Hôpital Armand Trousseau

References

Explore related publications, articles, or registry entries linked to this study.

Rigouzzo A, Louvet N, Favier R, Ore MV, Piana F, Girault L, Farrugia M, Sabourdin N, Constant I. Assessment of Coagulation by Thromboelastography During Ongoing Postpartum Hemorrhage: A Retrospective Cohort Analysis. Anesth Analg. 2020 Feb;130(2):416-425. doi: 10.1213/ANE.0000000000004422.

Reference Type DERIVED
PMID: 31567472 (View on PubMed)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

ArmandTrousseau

Identifier Type: -

Identifier Source: org_study_id