A Phase 4 interventional study of Prasugrel and Ticagrelor in Myocardial Infarction (MI), sponsored by Instituto de Investigación Sanitaria de la Fundación Jiménez Díaz. Recruiting at 5 sites in 5 countries. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-09-09.
Sponsored by Instituto de Investigación Sanitaria de la Fundación Jiménez Díaz · Phase 4, Interventional, and Treatment
This study is testing different blood-thinning treatment strategies for people who have had a heart attack and were successfully treated with a coronary stent procedure (PCI). All strategies tested are already approved for this condition and used inversally. This study will define which of the approved strategies is the best one.
After PCI, patients usually receive two antiplatelet medicines for up to 12 months to help prevent another heart attack or stroke, but this treatment can also increase bleeding risk. This study will compare a shorter course of dual antiplatelet therapy followed by one antiplatelet medicine alone versus the standard 12-month course. In addition, the study will compare two commonly used antiplatelet drugs, prasugrel and ticagrelor. The goal is to find out which strategy best prevents death, heart attack, or stroke while minimizing serious bleeding.
This study is not testing any new intervention, rather comparing approved drugs and approved durations of use.
Acute myocardial infarction (MI) remains associated with a substantial risk of recurrent ischemic events after successful percutaneous coronary intervention (PCI). Current standard treatment after MI and PCI includes dual antiplatelet therapy (DAPT), usually aspirin plus a potent P2Y12 inhibitor, to reduce the risk of death, recurrent MI, stroke, and stent thrombosis. However, longer DAPT duration is associated with increased bleeding risk, and the optimal balance between ischemic protection and bleeding safety remains uncertain. In addition, although prasugrel and ticagrelor are both recommended after MI, comparative randomized evidence remains limited in contemporary MI populations treated with PCI.
STREAMLINE is a pragmatic, multinational, multicenter, investigator-initiated, prospective, randomized, controlled, open-label trial with blinded endpoint adjudication (PROBE design). The study is designed to evaluate antiplatelet treatment strategies in patients with acute MI who have undergone successful index PCI. Approximately 8,100 participants will be enrolled across 65 sites in 6 European countries.
The trial uses a 2×2 factorial design and addresses 2 main treatment questions. First, the study will assess whether an abbreviated DAPT strategy is non-inferior to a standard 12-month DAPT strategy for the prevention of ischemic events at 12 months. In the abbreviated strategy, participants receive 1 to 3 months of DAPT followed by potent P2Y12 inhibitor monotherapy for the remainder of the first year. In the standard strategy, participants receive 12 months of DAPT. Second, the study will assess whether a prasugrel-based strategy is superior to a ticagrelor-based strategy in reducing ischemic events without increasing bleeding.
Eligible participants are adults hospitalized with acute MI who undergo successful PCI and dot not have a recommendation for anticoagulant therapy (eg atrial fibrillation or metalic valvular prostheses)). Randomization is performed anytime after successful index PCI and hospital discharge. Participants are first randomized 1:1 to prasugrel- or ticagrelor-based treatment and then randomized 2:1 to abbreviated or standard DAPT. All other treatments are prescribed according to routine clinical practice and the judgment of the treating physician. After 12 months, ongoing antiplatelet treatment is left to the discretion of the treating physician.
The primary efficacy endpoint is the composite of all-cause death, non-fatal MI, or stroke at 12 months, analyzed as time to first event. For the abbreviated-versus-standard DAPT comparison, the study will test non-inferiority. For the prasugrel-versus-ticagrelor comparison, the study will test superiority. The main safety endpoint is major bleeding at 12 months, defined as Bleeding Academic Research Consortium (BARC) type 3a to 5 bleeding. Secondary endpoints include individual components of the primary composite, cardiovascular death, net clinical benefit, and unplanned revascularization.
Participants will be followed for 12 months. Mandatory follow-up assessments will occur at 3 and 12 months, with additional follow-up, when feasible, at 1, 6, and 9 months. Follow-up will be performed by telephone contact and review of medical records to assess survival, hospitalizations, recurrent ischemic events, bleeding events, and adherence to the assigned antiplatelet strategy. No protocol-mandated laboratory testing or electrocardiographic assessments are required beyond routine care.
Potential endpoint events will be documented using source medical records and adjudicated centrally by an independent Clinical Events Adjudication Committee blinded to treatment allocation. The trial is intended to provide clinically relevant evidence under real-world conditions and to inform future guideline recommendations regarding the optimal type and duration of antiplatelet therapy after acute MI treated with PCI.
2,270 studies on the registry are indexed under Myocardial Infarction; 371 are open to participants now.
This study's planned enrollment of 8,100 is above the median of 150 across 1,314 interventional studies indexed under Myocardial Infarction.
Browse Myocardial Infarction studies →Instituto de Investigación Sanitaria de la Fundación Jiménez Díaz is the lead sponsor of 76 studies on the registry; 27 are open to participants now.
Counted across the registry records on this site, refreshed daily.
Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Exclusion Criteria:
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.
A “mini-stroke”: temporary stroke-like symptoms caused by reduced blood flow to part of the brain, spinal cord or eye, without signs of a new stroke on a scan.
Stroke symptoms need emergency care at once, even if they go away.
A score of how well the liver works in people with liver disease such as cirrhosis: class A is mild, B moderate and C severe.
CYP3A is a group of enzymes, mainly CYP3A4, in the liver and gut that break down many medicines. Some medicines, supplements and foods (grapefruit, St John’s wort) slow them down or speed them up, which changes how much of a study drug stays in the body.
Studies list them so they can be avoided or switched; bring a list of everything you take, including supplements.
The study doctor’s estimate of how long someone is likely to live. Criteria use it so that people can stay in the study long enough for it to answer its question.
Contraindication
A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
TIA (transient ischaemic attack)
A “mini-stroke”: temporary stroke-like symptoms caused by reduced blood flow to part of the brain, spinal cord or eye, without signs of a new stroke on a scan.
Stroke symptoms need emergency care at once, even if they go away.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Child-Pugh class
A score of how well the liver works in people with liver disease such as cirrhosis: class A is mild, B moderate and C severe.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
CYP3A (CYP3A4) inhibitors and inducers
CYP3A is a group of enzymes, mainly CYP3A4, in the liver and gut that break down many medicines. Some medicines, supplements and foods (grapefruit, St John’s wort) slow them down or speed them up, which changes how much of a study drug stays in the body.
Studies list them so they can be avoided or switched; bring a list of everything you take, including supplements.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Life expectancy
The study doctor’s estimate of how long someone is likely to live. Criteria use it so that people can stay in the study long enough for it to answer its question.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Prasugrel-based 12 months DAPT
Drug: Prasugrel
Prasugrel-Based DAPT for 1 to 3 Months, Followed by Prasugrel Monotherapy Through 12 Months After MI
Drug: Prasugrel
Ticagrelor-based 12 months DAPT
Drug: Ticagrelor
Ticagrelor-Based DAPT for 1 to 3 Months, Followed by Prasugrel Monotherapy Through 12 Months After MI
Drug: Ticagrelor
Prasugrel during 12 months
Ticagrelor plus aspirin
ischemic events
incidence of the composite of "all-cause death, reinfarction or stroke"
Time frame: 12 months
All-cause death
incidence of death from any cause
Time frame: 12 months
Reinfarction
incidence of non fatal reinfarction
Time frame: 12 months
stroke
incidence of stroke (ischemic or hemorrhagic)
Time frame: 12 months
cardiovascular death
incidence of detah from cardiovascular cause
Time frame: 12 months
Unplanned revascularization
incidence of revascularization that was not planned at the time of index discharge
Time frame: 12 months
Net adverse clinical benefit
incidence of the composite of "all-cause mortality, non-fatal MI or stroke and the incidence of BARC 3-5 bleeding"
Time frame: 12 months
Safety outcome (bleeding)
incidence of major bleeding (defined as BARC 3-5)
Time frame: 12 months
Plan to share: No — Drugs are already approved for the indication.
No publications or documents are linked to this record.
Started Sep 2026 (actual). Primary completion is estimated for Jul 2029, 34 months after the start.
Of 83 non-industry phase 4 interventional studies under Myocardial Infarction, half reached primary completion within 42 months of starting (the median), counting those still running; a quarter within 22 and three quarters within 78. This study's planned 34 months is below that.
Counting every sponsor, half of 87 studies reached it within 42 months; a quarter within 22 and three quarters within 78.
How these figures are worked out, and which studies are left out of them.
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Studies of the drugs tested here: Prasugrel · Ticagrelor
Instituto de Investigación Sanitaria de la Fundación Jiménez Díaz