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Completed

NCT Number: NCT00126334

Conservative Versus Liberal Red Cell Transfusion in Myocardial Infarction Trial: The CRIT Pilot

The purpose of this trial is to determine whether a conservative or a liberal blood transfusion strategy is better for patients with a heart attack and a low blood count.

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Key information

Age range

21 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Washington Hospital Center, Washington D.C., District of Columbia, United States

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About this study

The current standard of care for patients with heart attacks is to transfuse red blood cells when the hematocrit (red blood cell count) drops below 30 percent. However, there is little scientific basis for this current standard, and recent research has demonstrated that it is safe to allow the hematocrit (red blood cell count) to drop significantly lower in severely ill medical patients and in patients with heart disease undergoing major surgery. The investigators therefore propose this pilot trial to begin to determine whether or not it is safe to apply a more conservative blood transfusion strategy to patients with heart attacks.

In this study, patients who are within 72 hours of the onset of a heart attack and who are anemic (have a low red blood cell count) will be randomly assigned to one of two transfusion strategies while they are in the hospital: a liberal strategy of transfusing blood when the hematocrit falls below 30 percent (the current standard) or a conservative strategy of transfusing blood only when the hematocrit falls below 24 percent. It will then be determined which group fares better over the next 30 days.

The plan is to enroll 92 patients in this pilot trial in order to allow the researchers to plan for a much larger, definitive trial of this important question. It is anticipated that the conservative transfusion strategy will be similar to the standard (liberal) strategy in terms of patient outcomes.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

All of the following must be present:

  • Acute myocardial infarction with presentation within 72 hours of randomization (acute myocardial infarction is defined as ischemic-type chest discomfort lasting at least 30 minutes associated with creatinine kinase MB (CKMB) or troponin >upper limit of normal [ULN])
  • Admission to CCU
  • Hematocrit .30 or less
  • Written, informed consent

Exclusion criteria

  • Inability or unwillingness to receive red cell transfusions
  • Active bleeding (overt blood loss accompanied by a decrease in hematocrit of at least 5% in the preceding 12 hours)
  • Receipt of red cell transfusion within 7 days of randomization
  • Prior severe transfusion reaction
  • Pregnancy
  • Imminent death
  • Decision to provide limited care
  • Age <21
  • Participation in another clinical trial in which blood transfusion is a requirement or a component of a primary or secondary endpoint
  • Previous participation in the CRIT Pilot

Treatment and study plan

Packed Red Blood Cell Transfusion

Procedure

transfusion of 1 unit of PRBCs

Primary outcomes

  1. In-hospital death

    Time frame: In-hospital

  2. Recurrent myocardial infarction (MI)

    Time frame: In-hospital

  3. New or worsening heart failure

    Time frame: In-hospital

Secondary outcomes

  1. Critical Care Unit (CCU) length of stay

    Time frame: In-hospital

  2. Length of hospitalization

    Time frame: In-hospital

  3. Death or recurrent MI at hospital discharge and 30 days

    Time frame: 30 days

  4. Death or recurrent MI or new or worsening congestive heart failure (CHF) at 30 days

    Time frame: 30 days

  5. Death at 30 days

    Time frame: 30 days

  6. In-hospital recurrent ischemia

    Time frame: In-hospital

  7. In-hospital death or recurrent MI or new or worsening CHF or recurrent ischemia

    Time frame: In-hospital

  8. Acute renal insufficiency (increase in serum creatinine of ≥ 0.5mg/dL)

    Time frame: In-hospitall

  9. Number of transfusions received per patient

    Time frame: In-hospital

  10. Proportion of patients receiving at least one transfusion

    Time frame: In-hospital

  11. Mean daily hematocrit

    Time frame: In-hospital

  12. Transfusion-related reactions

    Time frame: In-hospital

Sponsors and collaborators

Lead sponsor

Medstar Health Research Institute

Other

Collaborators

  • US Department of Veterans Affairs

Registry information

Acronym: CRIT

Important dates

Study start
2003
Primary completion
2010
Study completion
2011
First posted
Aug 3, 2005
Registry last updated
Jul 21, 2011

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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