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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03075774
Other study ID # FibCard-N°RCB : 2016-A01995-46
Secondary ID
Status Not yet recruiting
Phase N/A
First received March 6, 2017
Last updated March 8, 2017
Start date March 2017
Est. completion date April 2018

Study information

Verified date March 2017
Source Société Française d'Anesthésie et de Réanimation
Contact Longrois Dan, Pr
Email dan.longrois@aphp.fr
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Multicenter prospective observational study, involving all adult patients who underwent cardiac surgery with extracorporeal circulation


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 3000
Est. completion date April 2018
Est. primary completion date April 2018
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patient over the age of 18 that underwent a cardiac surgery with extracorporeal circulation.

- Patient who agreed to participate in the study.

Exclusion Criteria:

- Patient under the age of 18.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Société Française d'Anesthésie et de Réanimation Keyrus Biopharma

Outcome

Type Measure Description Time frame Safety issue
Primary The international recommendations published by ESA in 2016 Review the concordance between the presence / absence of indication (according to the international recommendations published by ESA in 2016) and the prescription / non-prescription of fibrinogen concentrates 13 Months
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