Ischemia driven (FFR) complete percutaneous revascularisation of all significant stenosis in the non-culprit lesion performed within the index PCI procedure will improve clinical outcomes compared to the usual care, guided by discretion of the…
ID
Bron
Verkorte titel
Aandoening
coronary artery disease; NSTEMI; non ST-elevation myocardial infarction; multivessel disease; fractional flow reserve; FFR; culprit lesion; coronairlijden; non ST-elevatie myocardinfarct; meervatslijden
Ondersteuning
and
Maastricht University Medical Centre +, Maastricht, The Netherlands
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Primary study endpoints are defined as the incidence of MACE (Composite endpoint of all cause death, non-fatal Myocardial Infarction, any revascularisation and stroke) at 12 months.
Doel van het onderzoek
Ischemia driven (FFR) complete percutaneous revascularisation of all significant stenosis in the non-culprit lesion performed within the index PCI procedure will improve clinical outcomes compared to the usual care, guided by discretion of the physician.
Onderzoeksopzet
Time line
Initial enrolment May 2018
Last enrolment May 2020
One-year follow-up May 2019
Three year follow-up May 2023
Follow-up
For endpoint adjudication office-based direct visits will be performed at 1, 12 month and telephone-based interviews will be performed at 24 and 36 months.
Onderzoeksproduct en/of interventie
Patients will be enrolled and randomised in a 1:1 fashion between the ischemia driven (FFR) revascularisation strategy, versus usual care, after completion of a successful culprit lesion PCI. All patients who present at least with one lesion with a stenosis of approximately 50% or more in a non-IRA with a diameter of ≥ 2.0 mm and fulfil the inclusion and exclusion criteria will be enrolled.
Publiek
Wetenschappelijk
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
• Patients aged between 18-85 years presenting with non-STEMI according to current guidelines, who will be treated with PCI of the culprit and have at least one stenosis of >50% in a non-IRA on QCA or visual estimation of baseline angiography and judged feasible for treatment with PCI by the operator.
• Non-IRA stenosis amenable for PCI treatment (operator’s decision)
• Signed informed consent
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
1. Left main disease (stenosis > 50%)
2. Chronic total occlusion of a non-IRA
3. Indication for or previous coronary artery bypass grafting
4. Uncertain culprit lesion
5. Complicated IRA treatment, e.g. extravasation, permanent no re-flow after IRA treatment (TIMI flow 0-1) and inability to implant a stent
6. Known severe cardiac valve dysfunction that will require surgery or TAVI in the follow-up period.
7. Killip class III or IV during the completion of culprit lesion treatment.
8. Life expectancy of < 1 year.
9. Intolerance to Aspirin, Clopidogrel, Plasugrel, Ticagrelor or Heparin.
10. Gastrointestinal or genitourinary bleeding within the prior 3 months.
11. Planned elective surgical procedure necessitating interruption of thienopyridines during the first 6 months post enrolment.
12. Patients who are actively participating in another drug or device investigational study, which have not completed the primary endpoint follow-up period.
13. Pregnancy
Opzet
Deelname
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
Geen registraties gevonden.
Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
| Register | ID |
|---|---|
| NTR-new | NL6970 |
| NTR-old | NTR7158 |
| Ander register | : 17-T-142 |