Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT06601582

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

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

60

Participants Needed

1

Research Sites

143 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

Official 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 coronary artery bypass grafting (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 with hemoglobin less than 10 g/dl
  • Thrombocytopenia with platelet count less than 100,000/mm3
  • Coagulopathy with RNI greater than 1.5

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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2
3
+1

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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