Utility of Point-of-care Device for Rapid Determination of Cogulopathy in Trauma Patients

NCT ID: NCT02869737

Last Updated: 2016-08-17

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

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Recruitment Status

COMPLETED

Total Enrollment

100 participants

Study Classification

OBSERVATIONAL

Study Start Date

2015-01-31

Study Completion Date

2016-06-30

Brief Summary

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Traumatic coagulopathy is frequent and is an independent risk factor of mortality. Its detection mainly relies upon classic biological test like the prothrombin time and the international normaliezd ratio (INR). These tests are not available at the bedside. Point of care (POC) device for INR measurement are now available like the Coaguchek, Roche, France. The aim of the present study is to test the correlation between the POC INR and the laboratory INR.

Detailed Description

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Conditions

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Severe Trauma

Study Design

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Study Time Perspective

PROSPECTIVE

Interventions

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Coagucheck, Roche, France

Capillary puncture for POC INR measurement

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Age \> 15 y-o
* Admission for severe trauma

Exclusion Criteria

* Patients under oral anticoagulant
Minimum Eligible Age

15 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University Hospital, Grenoble

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

References

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Mistral T, Boue Y, Bosson JL, Manhes P, Greze J, Brun J, Albaladejo P, Payen JF, Bouzat P. Performance of point-of-care international normalized ratio measurement to diagnose trauma-induced coagulopathy. Scand J Trauma Resusc Emerg Med. 2017 Jun 21;25(1):59. doi: 10.1186/s13049-017-0404-y.

Reference Type DERIVED
PMID: 28637514 (View on PubMed)

Other Identifiers

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CECIC 2015-03

Identifier Type: -

Identifier Source: org_study_id

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