FAIO: The Use Of FFR Guided PCI Versus Complete Revascularization and Treatment Of Infarct Related Artery Only In Patients With STEMI

Sponsor
University of Limerick (Other)
Overall Status
Unknown status
CT.gov ID
NCT02637440
Collaborator
(none)
560
2
3
47
280
6

Study Details

Study Description

Brief Summary

In patients with ST elevation myocardial infarction (STEMI) the treatment goal is revascularization of the occluded artery with the use of primary percutaneous coronary intervention (PCI). There is a large subset of patients with STEMI who also have significant disease in arteries other than the site of occlusion, and away from the culprit artery. It is estimated that up to 50% have disease of more than 50% in the non-culprit arteries.

The evidence on how to treat those patients with multi vessel disease is conflicting. Earlier large-scale studies and registries have suggested early and complete revascularization is of no benefit or even harmful. More recent studies have showed the opposite of that. The CVLPRIT study showed that early complete revascularization or preventive PCI reduced primary endpoint of a composite of all cause mortality, myocardial infarction and need for repeat revascularization. The benefit was mainly due to reduced repeat revascularization in the more intensive intervention group. The PRAMI study showed very similar results as well.

The use of Fractional flow Reserve (FFR) in deciding complete revascularization has also showed conflicting results so far. A previous trial showed that FFR guided intervention post STEMI increased MACE. This was conflicted with more recent study, which showed FFR guided complete revascularization improved outcome when compared with more conservative treatment of ischaemia driven intervention.

In this study, the investigators are going to assess the issue of staged revascularization guided by FFR or by angiogram, compared to the standard treatment of ischaemia driven revascularization

Condition or Disease Intervention/Treatment Phase
  • Procedure: FFR guided PCI
  • Procedure: Angio guided PCI
Phase 3

Detailed Description

To compare the clinical outcomes measured by composite of mortality, myocardial infarction and repeat revascularization by using FFR guided and angiographically guided revascularization to the standard strategy of ischaemia driven revascularization.

Participants will be allocated to three arms, first conservative group of ischaemia guided PCI, second FFR guided PCI and third angiogram guided PCI where patients where patients with more than 50% lesion will undergo revascularization.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
560 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Multi Centre Open Label Randomised Controlled Parallel-group Three Arm Trial To Compare The Use Of Fractional Flow Reserve (FFR) Guided and Angiographically Guided Revascularization To The Treatment Of Infarct Related Artery Only In Patients With STEMI And Multivessel Disease
Study Start Date :
Dec 1, 2015
Anticipated Primary Completion Date :
Nov 1, 2019
Anticipated Study Completion Date :
Nov 1, 2019

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Conservative

After the index primary PCI. The control group will receive best medical therapy and regular follow up and only PCI for recurrent angina with evidence of inducible ischaemia.

Active Comparator: FFR guided

FFR group will undergo FFR at 4 weeks of the index primary PCI as OPD. If FFR is less than 0.8, then PCI will be performed

Procedure: FFR guided PCI
Patients undergo Fractional Flow measurement (FFR) followed by PCI, if the FFR is less than 0.8

Active Comparator: angiogram guided

The group will undergo PCI for all significant lesions more than 50

Procedure: Angio guided PCI
Patients receive PCI without FFR measurement

Outcome Measures

Primary Outcome Measures

  1. Composite of cardiovascular death, myocardial infarction and / or revascularization [1 year]

Secondary Outcome Measures

  1. Cardiovascular morality [1 year]

  2. Myocardial infarction [1 year]

  3. Revascularization [1 year]

    Revascularization procedure because of symptoms and evidence of ischaemia

  4. stroke [1 year]

  5. Heart failure [1 year]

    documented episode of presentation with symptoms consistent with heart failure and evidence from echocardiogram or laboratory test consistent with the diagnosis of heart failure

  6. Costs [1 year]

    total procedural costs, hospital stay costs, medications costs.

Other Outcome Measures

  1. Bleeding [1 year]

    any major bleeding (TIMI 3)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Patients with STEMI and multi-vessel disease on initial angiogram.

  2. Above 18 years of age

  3. Able to give consent

Exclusion Criteria:
  1. Patients with indication for CABG

  2. Left main stem lesion of >50%

  3. Cardiogenic shock

  4. Intractable angina during hospital admission

  5. Patients with limited life expectancy

  6. Patients with severe chronic kidney disease

  7. Patients with contraindication to dual antiplatelet therapy

  8. Patients with very complex lesions that deemed not favourable for PCI

  9. Pregnancy or childbearing age

Contacts and Locations

Locations

Site City State Country Postal Code
1 Galway University Hospital Galway Ireland
2 University Hospital Limerick Limerick Ireland 000

Sponsors and Collaborators

  • University of Limerick

Investigators

  • Principal Investigator: Thomas J Kiernan, MD, University Hospital of Limerick

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
A Abdullah, Dr., University of Limerick
ClinicalTrials.gov Identifier:
NCT02637440
Other Study ID Numbers:
  • FA 2015
First Posted:
Dec 22, 2015
Last Update Posted:
Dec 23, 2015
Last Verified:
Dec 1, 2015

Study Results

No Results Posted as of Dec 23, 2015