Overview

This trial is active, not recruiting.

Conditions myocardial infarction, cardiovascular disease
Treatments 6 months dapt, 12 months dapt
Phase phase 4
Sponsor Maasstad Hospital
Collaborator Medtronic
Start date December 2011
End date August 2017
Trial size 1100 participants
Trial identifier NCT01459627, DAPT-STEMI

Summary

OBJECTIVE OF THE STUDY: To test the hypothesis that 6 months DAPT (Dual anti-platelet therapy) after second generation DES (Drug Eluting Stent) implantation in STEMI (ST elevation Myocardial Infarction) is not inferior to 12 months DAPT in terms of clinical outcomes (composite endpoint of all-cause mortality, any MI, any revascularization, stroke and major bleeding at 18 months after randomization).

The trial will incorporate two registers studying respectively the safety outcomes of Bivalirudin and Prasugrel combination and Bivalirudin and Ticagrelor combination at 2 and 30 days. Finally the trial design permits assessment of the clinical outcomes after primary PCI for treatment of STEMI with the new Resolute Integrity (Medtronic Santa Rosa Ca, USA) stent at 30 days and 6 months.

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Allocation randomized
Endpoint classification safety/efficacy study
Intervention model parallel assignment
Masking open label
Primary purpose treatment
Arm
(Active Comparator)
Dual antiplatelet therapy consisting of aspirin (ASA) and prasugrel or ticagrelor will be discontinued after randomisation.
6 months dapt ticagrelor, prasugrel, ASA
Dual antiplatelet therapy will be stopped at randomisation to the 6 months DAPT group. Patients will be treated from 6 months onwards only with ASA.
(Active Comparator)
Dual antiplatelet therapy consisting of aspirin (ASA) and prasugrel or ticagrelor will be continued till 12 months after enrollment in the study
12 months dapt ticagrelor, prasugrel, ASA
Dual antiplatelet therapy will be continued till 12 months after enrollment in the study

Primary Outcomes

Measure
Net MACCE
time frame: 18 months

Secondary Outcomes

Measure
All cause mortality, MI, Stroke, ST and bleeding
time frame: 2 days
All cause mortality, MACCE, TIMI
time frame: 9 months
ST definite/probable
time frame: 9 months
all cause mortality
time frame: 9 months
Cardiac mortality
time frame: 9 months
MI
time frame: 9 months
Target vessel MI
time frame: 9 months
Bleeding
time frame: 9 months
stroke
time frame: 9 months
Target vessel revascularization
time frame: 9 months
Target lesion revascularization
time frame: 9 months
Target vessel failure
time frame: 9 months
Target lesion failure
time frame: 9 months
net MACCE
time frame: 30days
All cause mortality, MI, Stroke, ST and bleeding
time frame: 30 days
net MACCE
time frame: 6 months
All cause mortality, MACCE, TIMI
time frame: 18 months
ST definite/probable
time frame: 18 months
All cause mortality
time frame: 18 months
Cardiac mortality
time frame: 18 months
MI
time frame: 18 months
Target vessel MI
time frame: 18 months
Bleeding
time frame: 18 months
Stroke
time frame: 18 months
Target vessel revascularization
time frame: 18 months
Target lesion revascularization
time frame: 18 months
Target vessel failure
time frame: 18 months
Target lesion failure
time frame: 18 months
ST following ARC
time frame: 2 days
ST following ARC
time frame: 30 days
All cause mortality
time frame: 2 days
All cause mortality
time frame: 30 days
Cardiac mortality
time frame: 2 days
Cardiac Mortality
time frame: 30 days
All MI
time frame: 2 days
All MI
time frame: 30 days
Target vessel MI
time frame: 2 days
Target vessel MI
time frame: 30 days
Bleeding BARC
time frame: 2 days
Bleeding (BARC)
time frame: 30 days
Stroke
time frame: 2 days

Eligibility Criteria

Male or female participants from 18 years up to 85 years old.

Inclusion Criteria: STEMI patients between 18-85 years who underwent primary PCI with DES implantation. Exclusion criteria enrolment: - Intolerance to Aspirin, Prasugrel, Ticagrelor, Heparin, Bivalirudin, Zotarolimus or Everolimus. - Known bleeding diathesis or known coagulopathy. - Planned elective surgical procedure necessitating interruption of dual antiplatelet therapy during the first 6 months after randomization. - History of stent thrombosis - DES in main left coronary artery - Active bleeding, known bleeding diathesis or known coagulopathy. - Planned elective surgical procedure necessitating interruption of dual antiplatelet therapy during the first 6 months after randomization. - Oral anticoagulant therapy with Coumadin derivates - Malignancies or other comorbidity with a life expectancy of less than one year or that may result in protocol noncompliance - Pregnancy (present, suspected or planned) or positive pregnancy test (in women with childbearing potential a negative pregnancy test is mandatory) Exclusion criteria randomization: - Occurrence of death, myocardial infarction, stent thrombosis and target vessel or lesion revascularization during the first 6 months after inclusion. - Stroke or bleeding requiring discontinuation of DAPT during the first 6 months after inclusion. - Oral anticoagulant therapy Registry Exclusion criteria - Intolerance to Prasugrel, Ticagrelor, Bivalirudin. - Known bleeding diathesis or known coagulopathy Report Resolute Integrity Exclusion criteria • See exclusion criteria enrollment DAPT-STEMI protocol

Additional Information

Official title Prospective, Randomized, Open Label Trial of 6 Months vs. 12 Months Dual Antiplatelet Therapy After Drug-Eluting Stent Implantation In ST-elevation Myocardial Infarction
Principal investigator Elvin Kedhi, MD PHD
Description BACKGROUND OF THE STUDY: First generation DES (Drug Eluting Stents) have significantly reduced the restenosis rates compared to the BMS (Bare Metal Stents) but have raised concerns regarding higher rates and ongoing propensity for stent thrombosis. Based on these concerns current guidelines advocate dual antiplatelet therapy (DAPT, aspirin plus P2Y12 inhibitor) to be continued for up to 1 year after DES implantation. Large registries analyzing recent data now challenge these recommendations and suggest no increase in mortality or (late) stent thrombosis when DAPT is discontinued after 6 months. STUDY DESIGN: This is a prospective, randomized, open-label trial testing the hypothesis that 6 months DAPT after second generation drug eluting stent (DES) implantation in STEMI is not inferior to 12 months DAPT in terms of clinical outcomes. Patients with STEMI undergoing primary PCI will be enrolled at presentation. Only those patients who are event-free (death, MI, ST, TVR/TLR or unscheduled revascularization with DES in the first 6 months and stroke or bleeding requiring discontinuation of DAPT) and on DAPT at 6 months after primary PCI will be randomized (1:1 fashion) between single (aspirin) versus dual antiplatelet therapy (aspirin plus P2Y12) for an additional 6 months (up to 12 months after primary PCI) and assessed at 18 months post randomization. STUDY POPULATION: Patients between 18 and 85 years, presenting with STEMI undergoing PCI with DES implantation. INTERVENTION: Patients, who are event-free and stil on DAPT at 6 months after primary PCI will be randomized (1:1 fashion) between single (aspirin) versus dual antiplatelet therapy (aspirin plus P2Y12) for an additional 6 months (up to 12 months after primary PCI). PRIMARY STUDY PARAMETERS/OUTCOME OF THE STUDY: DAPT STEMI trial Composite endpoint of all cause mortality, any MI, any revascularization, stroke, ST and Bleeding (TIMI) (net MACCE) at 18 months after randomization. Registry Bivalirudin/Prasugrel and Bivalirudin/Ticagrelor All cause mortality, MI, Stroke, ST and bleeding (following BARC) at 2 and 30 days. Report Resolute Integrity Primary endpoint of DAPT-STEMI, at 30 days and 6 months.
Trial information was received from ClinicalTrials.gov and was last updated in December 2016.
Information provided to ClinicalTrials.gov by Maasstad Hospital.