NCT02648113

Brief Summary

Anemia in patients with myocardial infarction (MI) is a relatively frequent issue, resulting in poorer outcome. There is equipoise regarding which transfusion strategy is best, and there is an international consensus on the urgent need for a randomized trial. The investigators hypothesize that a "restrictive" transfusion strategy is at least non-inferior to a "liberal" transfusion strategy on 30-day outcomes of MI patients with anemia. Given the costs and risks of transfusion, a cost-effectiveness and cost-utility analysis becomes key to determining the role of each strategy.

Trial Health

90
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
668

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Mar 2016

Longer than P75 for not_applicable

Geographic Reach
2 countries

2 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

January 5, 2016

Completed
1 day until next milestone

First Posted

Study publicly available on registry

January 6, 2016

Completed
3 months until next milestone

Study Start

First participant enrolled

March 23, 2016

Completed
3.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 10, 2019

Completed
11 months until next milestone

Study Completion

Last participant's last visit for all outcomes

September 10, 2020

Completed
Last Updated

April 12, 2022

Status Verified

March 1, 2022

Enrollment Period

3.6 years

First QC Date

January 5, 2016

Last Update Submit

April 4, 2022

Conditions

Keywords

Myocardial InfarctionAnemiaBlood Transfusion

Outcome Measures

Primary Outcomes (1)

  • Cost-effectiveness ratio at 30 days

    The primary endpoint is the incremental cost-effectiveness ratio (ICER) at 30-days, using the composite endpoint (30-day composite of all-cause death, non fatal stroke, nonfatal recurrent MI, and emergency revascularization prompted by ischemia) as the effectiveness criterion

    30 days

Secondary Outcomes (3)

  • Cost-effectiveness ratio at 1 year

    1 year

  • Clinically non inferiority at 30 days

    30 days

  • Clinically non inferiority at 1 year

    1 year

Study Arms (2)

Restrictive transfusion strategy

EXPERIMENTAL

Transfusions are withheld unless Hb is \<= 8 g/dL, with a target Hb of 8 to 10 g /dL

Procedure: Restrictive transfusionBiological: red blood transfusion

Liberal transfusion strategy

EXPERIMENTAL

Transfusions are allowed as soon as Hb \<= 10 g/dL with a target of 11 g /dL.

Procedure: Liberal transfusionBiological: red blood transfusion

Interventions

Transfusions are withheld unless Hb is \<= 8 g/dL, with a target Hb of 8 to 10 g /dL

Restrictive transfusion strategy

transfusions are allowed as soon as Hb \<= 10 g/dL with a target of 11 g /dL

Liberal transfusion strategy
Liberal transfusion strategyRestrictive transfusion strategy

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Aged ≥ 18 years
  • Recent acute myocardial infarction, with or without ST- segment elevation, with a combination of ischemic symptoms occurring in the past 48 hours,before the MI related admission, and elevation of biomarkers of myocardial injury (troponin)
  • Anemia Hb ≤ 10g / dL but \> 7 g/dL on Hb, measured at any time during the index hospital admission for MI.
  • Written informed consent
  • Coverage for medical insurance.

You may not qualify if:

  • Shock (SBP \< 90 mmHg with clinical signs of low output or patients requiring inotropic agents)
  • MI occurring post-percutaneous coronary intervention (PCI) or post-coronary artery bypass graft (CABG) (i.e. type IV or V Acute MI according to the 2012 Universal Definition of MI
  • Life-threatening or massive ongoing bleeding (as judged by the investigator)
  • Any blood transfusion in the previous 30-days

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

Hôpital Bichat

Paris, France

Location

Hospital Clinic of Barcelona

Barcelona, 08036, Spain

Location

Related Publications (45)

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    PMID: 21873419BACKGROUND
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    PMID: 22922414BACKGROUND
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    PMID: 9971864BACKGROUND
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    PMID: 11246298BACKGROUND
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    PMID: 23281973BACKGROUND
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    PMID: 23380974BACKGROUND
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  • Ducrocq G, Gonzalez-Juanatey JR, Puymirat E, Lemesle G, Cachanado M, Durand-Zaleski I, Arnaiz JA, Martinez-Selles M, Silvain J, Ariza-Sole A, Ferrari E, Calvo G, Danchin N, Avendano-Sola C, Frenkiel J, Rousseau A, Vicaut E, Simon T, Steg PG; REALITY Investigators. Effect of a Restrictive vs Liberal Blood Transfusion Strategy on Major Cardiovascular Events Among Patients With Acute Myocardial Infarction and Anemia: The REALITY Randomized Clinical Trial. JAMA. 2021 Feb 9;325(6):552-560. doi: 10.1001/jama.2021.0135.

  • Ducrocq G, Calvo G, Gonzalez-Juanatey JR, Durand-Zaleski I, Avendano-Sola C, Puymirat E, Lemesle G, Arnaiz JA, Martinez-Selles M, Rousseau A, Cachanado M, Vicaut E, Silvain J, Karam C, Danchin N, Simon T, Steg PG; REALITY investigators. Restrictive vs liberal red blood cell transfusion strategies in patients with acute myocardial infarction and anemia: Rationale and design of the REALITY trial. Clin Cardiol. 2021 Feb;44(2):143-150. doi: 10.1002/clc.23453. Epub 2021 Jan 6.

  • Carson JL, Stanworth SJ, Dennis JA, Fergusson DA, Pagano MB, Roubinian NH, Turgeon AF, Valentine S, Trivella M, Doree C, Hebert PC. Transfusion thresholds and other strategies for guiding red blood cell transfusion. Cochrane Database Syst Rev. 2025 Oct 20;10(10):CD002042. doi: 10.1002/14651858.CD002042.pub6.

  • Radford M, Estcourt LJ, Sirotich E, Pitre T, Britto J, Watson M, Brunskill SJ, Fergusson DA, Doree C, Arnold DM. Restrictive versus liberal red blood cell transfusion strategies for people with haematological malignancies treated with intensive chemotherapy or radiotherapy, or both, with or without haematopoietic stem cell support. Cochrane Database Syst Rev. 2024 May 23;5(5):CD011305. doi: 10.1002/14651858.CD011305.pub3.

  • Ducrocq G, Cachanado M, Simon T, Puymirat E, Lemesle G, Lattuca B, Ariza-Sole A, Silvain J, Ferrari E, Gonzalez-Juanatey JR, Martinez-Selles M, Lermusier T, Coste P, Vanzetto G, Cottin Y, Dillinger JG, Calvo G, Steg PG; REALITY Investigators. Restrictive vs Liberal Blood Transfusions for Patients With Acute Myocardial Infarction and Anemia by Heart Failure Status: An RCT Subgroup Analysis. Can J Cardiol. 2024 Sep;40(9):1705-1714. doi: 10.1016/j.cjca.2024.02.013. Epub 2024 Feb 24.

  • Durand-Zaleski I, Ducrocq G, Mimouni M, Frenkiel J, Avendano-Sola C, Gonzalez-Juanatey JR, Ferrari E, Lemesle G, Puymirat E, Berard L, Cachanado M, Arnaiz JA, Martinez-Selles M, Silvain J, Ariza-Sole A, Calvo G, Danchin N, Paco S, Drouet E, Abergel H, Rousseau A, Simon T, Steg PG. Economic evaluation of restrictive vs. liberal transfusion strategy following acute myocardial infarction (REALITY): trial-based cost-effectiveness and cost-utility analyses. Eur Heart J Qual Care Clin Outcomes. 2023 Feb 28;9(2):194-202. doi: 10.1093/ehjqcco/qcac029.

  • Carson JL, Stanworth SJ, Dennis JA, Trivella M, Roubinian N, Fergusson DA, Triulzi D, Doree C, Hebert PC. Transfusion thresholds for guiding red blood cell transfusion. Cochrane Database Syst Rev. 2021 Dec 21;12(12):CD002042. doi: 10.1002/14651858.CD002042.pub5.

MeSH Terms

Conditions

Myocardial InfarctionAnemia

Interventions

Erythrocyte Transfusion

Condition Hierarchy (Ancestors)

Myocardial IschemiaHeart DiseasesCardiovascular DiseasesVascular DiseasesInfarctionIschemiaPathologic ProcessesPathological Conditions, Signs and SymptomsNecrosisHematologic DiseasesHemic and Lymphatic Diseases

Intervention Hierarchy (Ancestors)

Blood Component TransfusionBlood TransfusionBiological TherapyTherapeutics

Study Officials

  • Philippe-Gabriel STEG

    Assistance Publique - Hôpitaux de Paris

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 5, 2016

First Posted

January 6, 2016

Study Start

March 23, 2016

Primary Completion

October 10, 2019

Study Completion

September 10, 2020

Last Updated

April 12, 2022

Record last verified: 2022-03

Locations