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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 19 February 2015
Main ID:  NCT00772239
Date of registration: 13/10/2008
Prospective Registration: No
Primary sponsor: University Hospital, Limoges
Public title: Perioperative Coagulation Management in Cardiac Surgery. ROTEM
Scientific title: Perioperative Coagulation Management in Cardiac Surgery. Rotem Versus Standard Pratctice. A Randomized Trial.
Date of first enrolment: October 2008
Target sample size: 100
Recruitment status: Terminated
URL:  http://clinicaltrials.gov/show/NCT00772239
Study type:  Interventional
Study design:  Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Health Services Research  
Phase:  N/A
Countries of recruitment
France
Contacts
Name:     Nathalie NATHAN-DENIZOT, MD
Address: 
Telephone:
Email:
Affiliation:  CHU limoges
Key inclusion & exclusion criteria

Inclusion Criteria:

- Adults> 18 years

- Cardiac surgery or heart transplantation with abnormal bleeding regardless the
etiology

- given informed consent

Exclusion Criteria:

- Patient supported by a pre or postoperative circulatory technical assistance



Age minimum: 18 Years
Age maximum: N/A
Gender: Both
Health Condition(s) or Problem(s) studied
Bleeding
Cardiac Surgery
Intervention(s)
Procedure: Standard coagulation managment procedure
Device: Rotation thromboelastometry (ROTEM)
Primary Outcome(s)
Quantity of different blood transfusion [Time Frame: during cardiac surgery management]
Secondary Outcome(s)
Secondary ID(s)
I07018/ROTEM CTV
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Laboratoire français de Fractionnement et de Biotechnologies
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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