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NCT01870063 Clinical Trial

Comparision of FIBTEM and Blood-loss

Sternotomy Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01870063
Other study ID # BLUTROT
Secondary ID
Status Completed
Phase N/A
First received June 3, 2013
Last updated August 5, 2014
Start date June 2013
Est. completion date August 2014

Study information
Verified date August 2014
Source Johann Wolfgang Goethe University Hospitals
Contact n/a
Is FDA regulated No
Health authority Germany: Ethics Commission
Study type Observational [Patient Registry]

Clinical Trial Summary

Correlation between FIBTEM and intraoperative blood loss

Recruitment information / eligibility
Status Completed
Enrollment 71
Est. completion date August 2014
Est. primary completion date August 2014
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria:

full sternotomy age >18 Inform consent signed

Exclusion Criteria:

Hypofibrinogen

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
Germany Goethe University Hospital Frankfurt Hessen

Sponsors (1)
Lead Sponsor Collaborator
Johann Wolfgang Goethe University Hospitals

Country where clinical trial is conducted

Germany, 

Outcome
Type Measure Description Time frame Safety issue
Primary bleeding intraoperative Yes
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