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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02981407
Other study ID # Pro20160000722
Secondary ID 1U01HL133817-01
Status Completed
Phase Phase 3
First received
Last updated
Start date April 25, 2017
Est. completion date October 20, 2023

Study information

Verified date April 2024
Source Rutgers, The State University of New Jersey
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to compare two red blood cell transfusion strategies (liberal and restrictive) for patients who have had an acute myocardial infarction and are anemic.


Description:

In most clinical settings, evidence suggests it is safe to wait to give a blood transfusion. However, for those who have suffered a heart attack, there is a lack of high quality evidence to guide transfusions. This 3500 subject multi-center randomized trial will fill that void. Hospital inpatients diagnosed with myocardial infarction who have blood counts less than 10 g/dL are randomized to receive either a liberal or a restrictive transfusion strategy. Patients randomized to the liberal transfusion strategy will receive a red blood cell transfusion anytime there is a blood count of less than 10 g/dL. Patients randomized to the restrictive transfusion strategy are permitted to receive a blood transfusion if the blood count is below 8 g/dL and the physician believes it is in the patient's best interest. A transfusion will be strongly recommended if the blood count drops to less than 7 g/dL. If the patient has symptoms of angina (e.g., chest discomfort described as pressure or heaviness) that do not go away with medication, a blood transfusion is ordered regardless of the blood count. The transfusions strategies will be maintained until hospital discharge for a maximum of 30 days. Patients will be followed for 30 days for clinically relevant outcomes. Vital status will be confirmed at 180 days.


Recruitment information / eligibility

Status Completed
Enrollment 3506
Est. completion date October 20, 2023
Est. primary completion date May 31, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - 18 years of age or older - Either ST segment elevation myocardial infarction or Non ST segment elevation myocardial infarction consistent with the 3rd Universal Definition of Myocardial Infarction criteria that occurs on admission or during the index hospitalization - Hemoglobin concentration less than 10 g/dL at the time of random allocation - Patient physician believes that both of the transfusion strategies are consistent with good medical care for the patient Exclusion Criteria: - Uncontrolled acute bleeding at the time of randomization defined as the need for uncrossed or non-type specific blood - Decline blood transfusion - Scheduled for cardiac surgery during the current admission - Receiving only palliative treatment - Known that follow-up will not be possible at 30 days - Previously participated in MINT - Currently enrolled in a competing study that interferes with the intervention or follow-up of MINT or enrolled in a competing study that has not been approved by the local Institutional Review Board - Patient physician does not believe the patient is an appropriate candidate for the trial

Study Design


Intervention

Biological:
Red Blood Cell Transfusion
Transfusion of packed red blood cell units

Locations

Country Name City State
Australia Flinders Medical Centre Bedford Park
Australia Concord Repatriation General Hospital Concord
Australia Gosford Hospital Gosford
Australia Royal Perth Hospital Perth
Brazil Hospital Felício Rocho Belo Horizonte
Brazil Instituto Orizonti Belo Horizonte
Brazil Instituto de Ensino e Pesquisa do Hospital do Coração do Brasil Brasília
Brazil Hospital Vera Cruz Campinas
Brazil Santa Casa de Marília Cascata
Brazil Sociedade Hospitalar Angelina Caron Centro
Brazil Instituto de Ensino e Pesquisa do Hospital da Bahia Pituba Salvador
Brazil Hospital Maternidade e Pronto Socorro Santa Lúcia Poços De Caldas
Brazil Instituto de Cardiologia do RS Porto Alegre
Brazil Hospital Agamenon Magalhães Recife
Brazil Pronto Socorro Cardiológico de Pernambuco Prof. Luiz Tavares- PROCAPE Recife
Brazil Hospital Cárdio Pulmonar Salvador
Brazil Hospital Universitário Professor Edgard Santos Salvador
Brazil Hospital de Base de Rio Preto São José Do Rio Preto
Brazil Hospital de Base de Rio Preto São José do Rio Preto São Paulo
Brazil Hospital São Paulo São Paulo
Brazil Hospital de Clínicas da UFTM Uberaba
Brazil Hospital das Clinicas da UFU Uberlândia
Canada Foothills Medical Centre Calgary Alberta
Canada Grey Nuns Community Hospital Edmonton Alberta
Canada Royal Alexandra Hospital Edmonton Alberta
Canada University of Alberta Hospital Edmonton Alberta
Canada Hôpital Charles Lemoyne Greenfield Park Quebec
Canada QE II Health Sciences Center Halifax Nova Scotia
Canada Hamilton Health Sciences Hamilton Ontario
Canada Hamilton St. Joseph's Health Hamilton Ontario
Canada St. Joseph's Health Centre Hamilton Ontario
Canada Hotel-Dieu de Levis Levis Quebec
Canada University Hospital - LHSC London Ontario
Canada Victoria Hospital - LHSC London Ontario
Canada Jewish General Hospital Montreal Quebec
Canada Centre Hosp. Universitaire de Montréal Montréal Quebec
Canada Montreal General Hospital Montréal Quebec
Canada Royal Victoria Hospital Montréal Quebec
Canada Royal Columbian Hospital New Westminster British Columbia
Canada Quebec Heart and Lung Institute Québec City Quebec
Canada Regina General Hospital Regina Saskatchewan
Canada Centre Hospitalier Universitaire de Sherbrooke Sherbrooke Quebec
Canada Surrey Memorial Hospital Surrey British Columbia
Canada St. Michael's Hospital Toronto Ontario
Canada Sunnybrook Health Sciences Centre Toronto Ontario
Canada General Hospital Trois-Rivièrs Trois-Rivières Quebec
Canada Vancouver General Hospital Vancouver British Columbia
Canada Victoria Heart Institute Victoria Ontario
Canada St. Boniface General Hospital Winnipeg Manitoba
France CHRU Tours -Hôpital Trousseau Chambray-lès-Tours
France CH Chartres - Chartres Chartres
France Centre Hospitalier Sud Francilien Corbeil-Essonnes
France CHU le Bocage - Dijon Dijon
France La Tronche Hôpital Michallon La Tronche
France Centre Hospitalier Universitaire de Lille Lille
France CHU Arnaud de Villeneuve - Montpellier Montpellier
France CHU Nancy Nancy
France Hôpital Pasteur Nice
France Hôpital Universitaire Carémeau (CHU Carémeau) Nîmes
France Hôpital BICHAT- APHP Paris
France Hôpital Européen Georges-Pompidou Paris
France Hôpital La Pitié Salpétrière Paris
France Hôpital Lariboisière Paris
France Hôpital Haut Lévêque Pessac
France CHU Poitiers - Poitiers Poitiers
France Hôpital Charles Nicolle- Rouen Rouen
France Hôpital Rangueil Toulouse
New Zealand Auckland City Hospital Auckland
New Zealand Christchurch Hospital Christchurch
New Zealand Gisborne Hospital Gisborne
New Zealand Nelson Hospital Nelson
New Zealand Taranaki Hospital New Plymouth
New Zealand Whangarei Hospital Whangarei
United States Albany Medical College Albany New York
United States University of New Mexico Albuquerque New Mexico
United States University of Michigan Ann Arbor Michigan
United States Southside Hospital Bay Shore New York
United States Beth Israel Deaconess Medical Center Boston Massachusetts
United States Boston Medical Center Boston Massachusetts
United States Massachusetts General Hospital Boston Massachusetts
United States Montefiore Medical Center Bronx New York
United States NYP Brooklyn Methodist Brooklyn New York
United States Lahey Hospital Burlington Massachusetts
United States University of Vermont Medical Center Burlington Vermont
United States Copper University Hospital Camden New Jersey
United States Aultman Hospital Canton Ohio
United States The University of North Carolina at Chapel Hill Chapel Hill North Carolina
United States Rush University Medical Center Chicago Illinois
United States University of Chicago Medical Center Chicago Illinois
United States Danbury Hospital Danbury Connecticut
United States Essentia Health Duluth Minnesota
United States Durham Va Durham North Carolina
United States Alexian Brothers Medical Center Elk Grove Village Illinois
United States New York Presbyterian/Queens Flushing New York
United States Greenville Health System Greenville South Carolina
United States Memorial Hospital at Gulfport Gulfport Mississippi
United States Hackensacjk University Medical Center Hackensack New Jersey
United States Westchester Medical Center Hawthorne New York
United States AMITA Health Hinsdale Illinois
United States Baylor St Luke's Medical Center Houston Texas
United States Saint Luke's Mid America Heart Kansas City Kansas
United States Lancaster General Hospital Lancaster Pennsylvania
United States Central Arkansas Veterans Healthcare System Little Rock Arkansas
United States University of Arkansas Medical Sciences (UAMS) Hospital Little Rock Arkansas
United States VAGLAHS Los Angeles California
United States University of Louisville Louisville Kentucky
United States North Shore University Hospital Manhasset New York
United States The Memphis VAMC Memphis Tennessee
United States Medical College of Wisconsin - Froedtert Hospital Milwaukee Wisconsin
United States Minneapolis Heart Institute (Foundation) Minneapolis Minnesota
United States University of Minnesota Medical Center Fairview Minneapolis Minnesota
United States Northern Westchester Hospital Mount Kisco New York
United States Jersey Shore University Medical Neptune New Jersey
United States Robert Wood Johnson University Hospital New Brunswick New Jersey
United States Tulane University School of Medicine New Orleans Louisiana
United States Lenox Hilll Hospital New York New York
United States NYU Langone Medical Center, Bellevue Hospital New York New York
United States PENN Presbyterian Medical Cente Philadelphia Pennsylvania
United States Thomas Jefferson University Philadelphia Pennsylvania
United States University of Pittsburgh Medical Center Pittsburgh Pennsylvania
United States Rhode Island Hospital Providence Rhode Island
United States The Miriam Hospital Providence Rhode Island
United States WakeMed Health and Hospital Raleigh North Carolina
United States Virginia Commonwealth University Richmond Virginia
United States Mayo Clinic Rochester Minnesota
United States Rochester General Hospital Rochester New York
United States University of Rochester Rochester New York
United States Washington University Saint Louis Missouri
United States Northwell Staten Island Hopsital Staten Island New York
United States Stony Brook Medicine Stony Brook New York
United States University of Toledo Medical Center Toledo Ohio
United States Lankenau Medical Center Wynnewood Pennsylvania
United States St. Joseph Mercy Health System Ypsilanti Michigan

Sponsors (3)

Lead Sponsor Collaborator
Rutgers, The State University of New Jersey National Heart, Lung, and Blood Institute (NHLBI), University of Pittsburgh

Countries where clinical trial is conducted

United States,  Australia,  Brazil,  Canada,  France,  New Zealand, 

References & Publications (4)

Carson JL, Brooks MM, Abbott JD, Chaitman B, Kelsey SF, Triulzi DJ, Srinivas V, Menegus MA, Marroquin OC, Rao SV, Noveck H, Passano E, Hardison RM, Smitherman T, Vagaonescu T, Wimmer NJ, Williams DO. Liberal versus restrictive transfusion thresholds for patients with symptomatic coronary artery disease. Am Heart J. 2013 Jun;165(6):964-971.e1. doi: 10.1016/j.ahj.2013.03.001. Epub 2013 Apr 8. — View Citation

Carson JL, Brooks MM, Chaitman BR, Alexander JH, Goodman SG, Bertolet M, Abbott JD, Cooper HA, Rao SV, Triulzi DJ, Fergusson DA, Kostis WJ, Noveck H, Simon T, Steg PG, DeFilippis AP, Goldsweig AM, Lopes RD, White H, Alsweiler C, Morton E, Hebert PC; MINT Investigators. Rationale and design for the myocardial ischemia and transfusion (MINT) randomized clinical trial. Am Heart J. 2023 Mar;257:120-129. doi: 10.1016/j.ahj.2022.11.015. Epub 2022 Nov 20. — View Citation

Carson JL, Brooks MM, Hebert PC, Goodman SG, Bertolet M, Glynn SA, Chaitman BR, Simon T, Lopes RD, Goldsweig AM, DeFilippis AP, Abbott JD, Potter BJ, Carrier FM, Rao SV, Cooper HA, Ghafghazi S, Fergusson DA, Kostis WJ, Noveck H, Kim S, Tessalee M, Ducrocq G, de Barros E Silva PGM, Triulzi DJ, Alsweiler C, Menegus MA, Neary JD, Uhl L, Strom JB, Fordyce CB, Ferrari E, Silvain J, Wood FO, Daneault B, Polonsky TS, Senaratne M, Puymirat E, Bouleti C, Lattuca B, White HD, Kelsey SF, Steg PG, Alexander JH; MINT Investigators. Restrictive or Liberal Transfusion Strategy in Myocardial Infarction and Anemia. N Engl J Med. 2023 Dec 28;389(26):2446-2456. doi: 10.1056/NEJMoa2307983. Epub 2023 Nov 11. — View Citation

Carson JL, Guyatt G, Heddle NM, Grossman BJ, Cohn CS, Fung MK, Gernsheimer T, Holcomb JB, Kaplan LJ, Katz LM, Peterson N, Ramsey G, Rao SV, Roback JD, Shander A, Tobian AA. Clinical Practice Guidelines From the AABB: Red Blood Cell Transfusion Thresholds and Storage. JAMA. 2016 Nov 15;316(19):2025-2035. doi: 10.1001/jama.2016.9185. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Other Composite of All-cause Mortality,Nonfatal Myocardial Reinfarction, or Unstable Angina Within 30 days of randomization
Other Ischemia Driven Unscheduled Coronary Revascularization Within 30 days of randomization
Other Unscheduled Readmission to Hospital for Ischemic Cardiac Diagnosis Within 30 days of randomization
Other Heart Failure Within 30 days of randomization
Other Unscheduled Readmission to Hospital for Any Reason Within 30 days of randomization
Other Stroke Within 30 days of randomization
Other Pulmonary Embolism or Deep Venous Thrombosis Within 30 days of randomization
Other Bleed Within 30 days of randomization
Other Pneumonia Within 30 days of randomization
Other Blood Stream Infection Within 30 days of randomization
Other Urinary Tract Infection Within 30 days of randomization
Other Length of Hospital Stay Post Randomization Within 30 days of randomization
Other Number of Days Post Randomization in Intensive Care Unit Within 30 days of randomization
Other Patient Reported Quality of Life EuroQol questionnaire Within 30 days of randomization
Other All-cause Mortality Within 6 months of randomization
Primary Number of Participants With All-cause Mortality or Nonfatal Myocardial Reinfarction Within 30 days of randomization
Secondary All-cause Mortality Within 30 days of randomization
Secondary Myocardial Reinfarction Within 30 days of randomization
Secondary Composite of All-cause Mortality, Nonfatal Myocardial Reinfarction, Ischemia Driven Unscheduled Coronary Revascularization, or Readmission to the Hospital for Ischemic Cardiac Diagnosis Within 30 days of randomization
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