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NCT02712879 Clinical Trial

Moderate Bleeding in Cardiac Surgery Post Operative

Heart Surgery Clinical Trial

— SPO  

Official title:
Bleeding Moderate Postoperative Cardiac Surgery and Prognostic Implications Anemia and Postoperative Transfusion: Prospective, Observational, Descriptive.

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02712879
Other study ID # UF9695
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 11, 2016
Est. completion date June 30, 2016

Study information
Verified date April 2022
Source University Hospital, Montpellier
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Determine a bleeding threshold by measuring the blood volume in ml / kg / h collected in the drainage system to define moderate bleeding postoperative cardiac surgery and define the population.

Description:

Determine a bleeding threshold by measuring the blood volume in ml / kg / h collected in the drainage system to define moderate bleeding postoperative cardiac surgery and define the population. Secondary objectives: To evaluate the kinetics of moderate SPORT and its impact on anemia and postoperative transfusion. To evaluate the prognostic impact of the SPO moderate in terms of post-operative complications. Determine predictors of moderate SPO.

Recruitment information / eligibility
Status Completed
Enrollment 303
Est. completion date June 30, 2016
Est. primary completion date June 30, 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria: - Patients in the postoperative intensive care in cardiac surgery Exclusion Criteria: - Patients who received a heart transplant, a heart surgery beating, cardiac support establishment of long duration, or have a disease that alters the coagulation.

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
France UHMontpellier Montpellier

Sponsors (1)
Lead Sponsor Collaborator
University Hospital, Montpellier

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Evolution of blood loss per hour drains Hourly blood loss in drains during the first twelve hours Hourly blood loss in drains during the first twelve hours
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