Status:
UNKNOWN
Diagnostic Accuracy Study of a Point-of-Care Test for Coagulation Function
Lead Sponsor:
Hospital de Base
Conditions:
CoaguChek® XS System
Coagulation Function
Eligibility:
All Genders
18+ years
Brief Summary
Intraoperative coagulopathies in complex procedures are common. For the diagnosis and adequate therapy, laboratory tests are necessary, which can delay the patient's therapy. In this sense, the study ...
Detailed Description
Laboratory evaluation of blood clotting is widely used in perioperative medicine, either by conventional technique (prothrombin time - PT/INR, Activated Partial Thromboplastin Time - aPTT, fibrinogen ...
Eligibility Criteria
Inclusion
- patients over 18 years old
- admitted to the Hospital de Base of the Federal District for cardiac surgery, who volunteered to participate in the examination both by the traditional method of venous INR examination and by the use of the Coaguchek device and only after signing the TCLE.
Exclusion
- patients who give up the research even after signing the TCLE will be excluded
- patients who do not meet the aforementioned inclusion criteria
- patients who refuse to participate in the study
- patients with kidney, liver, hematological disease or any disease that affects coagulation
- patients participating in other studies
Key Trial Info
Start Date :
September 1 2023
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
January 1 2024
Estimated Enrollment :
50 Patients enrolled
Trial Details
Trial ID
NCT06037720
Start Date
September 1 2023
End Date
January 1 2024
Last Update
September 14 2023
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