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N/A

Transfusion for Heart Attack (MINT Trial)

N/A
Waitlist Available
Led By Paul Hébert, MD
Research Sponsored by Centre hospitalier de l'Université de Montréal (CHUM)
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up time frame: 6 months
Awards & highlights

MINT Trial Summary

This trial will compare two different strategies of blood transfusion for heart attack patients to see which is more effective.

Eligible Conditions
  • Heart Attack

MINT Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~time frame: 6 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and time frame: 6 months for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Enrollment rate
Non-adherence
Secondary outcome measures
Recurrent non-fatal myocardial infarction

Side effects data

From 2014 Phase 3 trial • 118 Patients • NCT00003138
31%
Fatigue
23%
Pulmonary
15%
Infection
8%
Cardiac adverse event
8%
Diarrhea
8%
Esophagitis
8%
Hot flashes
8%
Other toxicities
8%
Hemorrhage
8%
Skin
8%
Weight loss
8%
Neuropathy-clinical
8%
Edema
8%
Anemia
8%
Neuropathy-psych
8%
Abdominal cramps
100%
80%
60%
40%
20%
0%
Study treatment Arm
Erythropoietin (300 Units/kg) and Filgrastim (Step 4)
Supportive Care (Step 1)
Erythropoietin (Step 1)
Erythropoietin (Cross-over; Step 2)
Erythropoietin (150 Units/kg) and Filgrastim (Step 3)

MINT Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Restrictive Transfusion StrategyExperimental Treatment1 Intervention
We will permit but not require red cell transfusions once a hemoglobin value falls below 80 g/L (required below 70 g/L) during the 30 days following randomization
Group II: Liberal Transfusion StrategyActive Control1 Intervention
We will transfuse at a transfusion threshold of 100 g/L for up to 30 days after randomization.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Transfusion
2021
Completed Phase 3
~7150

Find a Location

Who is running the clinical trial?

Centre hospitalier de l'Université de Montréal (CHUM)Lead Sponsor
366 Previous Clinical Trials
126,136 Total Patients Enrolled
Canadian Blood ServicesOTHER
20 Previous Clinical Trials
17,138 Total Patients Enrolled
Canadian Institutes of Health Research (CIHR)OTHER_GOV
1,341 Previous Clinical Trials
26,449,212 Total Patients Enrolled

Media Library

Transfusion (N/A) Clinical Trial Eligibility Overview. Trial Name: NCT02619136 — N/A
Heart Attack Research Study Groups: Restrictive Transfusion Strategy, Liberal Transfusion Strategy
Heart Attack Clinical Trial 2023: Transfusion Highlights & Side Effects. Trial Name: NCT02619136 — N/A
Transfusion (N/A) 2023 Treatment Timeline for Medical Study. Trial Name: NCT02619136 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Does this investigation currently accept enrollees?

"As confirmed on clinicaltrials.gov, this medical trial is not currently looking for enrollees. This particular study was initially announced on June 30th 2016 and its latest update took place in July 24th 2023. Although it has now concluded recruitment, there are 1162 other trials actively seeking participants at the moment."

Answered by AI

Could you provide a detailed account of the number of sites that are presently running this investigation?

"Currently, 4 medical centres are enrolling patients for this clinical trial. These include Victoria Heart Institute in Victoria, Centre Hospitalier de l'Universite de Montreal-Hotel Dieu in Montreal, and Institut Universitaire de Cardiologie et Pneumologie in Quebec City as well as other sites scattered throughout the country."

Answered by AI
~400 spots leftby Apr 2025