Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
ID06601582

Effectiveness of a Intraoperative Blood Recovery System in Cardiovascular Surgery Using Cardiopulmonary Bypass in Brazil. Randomized Crontrolled Trial

Led by Instituto Materno Infantil Prof. Fernando Figueira · Updated on 2024-09-19

60

Participants Needed

1

Research Sites

13 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Randomized trial to evaluate the effectiveness of a intra operative blood recovery system in reducing the need for allogeneic transfusion in cardiovascular surgeries using cardiopulmonary bypass

CONDITIONS

Brief Title

Effectiveness of a Intraoperative Blood Recovery System in Cardiovascular Surgery in Brazil

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • all patients undergoing CABG or Valve surgery singly.
Not Eligible

You will not qualify if you...

  • Emergency cardiac surgery;
  • Previous heart surgery;
  • End-stage chronic kidney disease;
  • Inability to receive a blood transfusion (refusal);
  • Anemia (hemoglobin less than 10g/dl);
  • Thrombocytopenia (platelet count less than 100,000/mm3);
  • Coagulopathy (RNI > 1.5);

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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2
3
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Trial Site Locations

Total: 1 location

1

Integral Medicine Institute Professor. Fernando Figueira-IMIP

Recife, Pernambuco, Brazil, 50070550

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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