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Evaluation of iFR vs FFR in Stable Angina or Acute Coronary Syndrome (iFR Swedeheart)

Primary Purpose

Angina Pectoris, Acute Myocardial Infarction

Status
Completed
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
iFR
FFR
Sponsored by
Uppsala University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Angina Pectoris focused on measuring Instantaneous wave Free Ratio, Fractional Flow Reserve

Eligibility Criteria

18 Years - 99 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with suspected stable angina pectoris or unstable angina pectoris/non-ST-segment elevation myocardial infarction (NSTEMI) who are scheduled to undergo coronary angiography, and who has an indication for physiology guided assessment of coronary lesions (usually 30-80% stenosis grade). In patients with suspected stable angina pectoris, any lesion may be assessed. In patients with unstable angina pectoris/NSTEMI, only the non-culprit lesion may be assessed.

Exclusion Criteria:

  • Inability to provide informed consent
  • Age below 18 years
  • Previous randomization in the iFR-SWEDEHEART trial
  • Known terminal disease with a life expectancy of less than one year.
  • In patients with multi-vessel disease and other indication than stable angina pectoris, difficulty in assessing which the culprit lesion is.
  • Patient with unstable hemodynamics (Killip class III-IV)
  • Inability to tolerate Adenosine
  • Previous Coronary artery bypass graft (CABG) with patent grafts to the interrogated vessel.
  • Heavily calcified or tortuous vessel where inability to cross the lesion with a pressure wire is expected.

Sites / Locations

  • Skejby University Hospital
  • Reykjavik University Hospital
  • Sahlgrenska University Hospital
  • Halmstad sjukhus
  • Helsingborg County Hospital
  • Kalmar County Hospital
  • Karlstad County Hospital
  • Linköping University Hospital
  • Skane University Hospital
  • S:t Göran County Hospital
  • Sundsvall County Hospital
  • Uppsala University Hospital
  • Västerås County Hospital
  • Örebro University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Instantaneous wave-free ratio (iFR)

Fractional Flow Reserve (FFR)

Arm Description

Outcomes

Primary Outcome Measures

All cause death, non-fatal Myocardial infarction (MI), Unplanned revascularization

Secondary Outcome Measures

All cause death
Non-fatal MI
Unplanned revascularization
Target lesion revascularization
Time to acute coronary occlusion, stent thrombosis and restenosis in treated lesions as reported in Swedish Coronary Angiography and Angioplasty Registry (SCAAR)
Change in physician´s treatment strategy depending on iFR/FFR information
Before randomization, the operators will have to record their angiographic assessment of the coronary lesions and the theoretical treatment strategy based on the angiographic information alone. After randomization and functional assessment of lesion severity, the operators will record how iFR/FFR changed the treatment strategy.
Assessment of patient discomfort during the procedure (none/mild/moderate/severe
Procedural time

Full Information

First Posted
May 7, 2014
Last Updated
January 11, 2017
Sponsor
Uppsala University
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1. Study Identification

Unique Protocol Identification Number
NCT02166736
Brief Title
Evaluation of iFR vs FFR in Stable Angina or Acute Coronary Syndrome
Acronym
iFR Swedeheart
Official Title
Instantaneous Wave-Free Ratio Versus Fractional Flow Reserve in Patients With Stable Angina Pectoris or Acute Coronary Syndrome. A Multicenter, Prospective, Randomized Controlled Clinical Trial Based on the Swedish Angiography and Angioplasty Registry (SWEDEHEART) Platform
Study Type
Interventional

2. Study Status

Record Verification Date
January 2017
Overall Recruitment Status
Completed
Study Start Date
May 2014 (undefined)
Primary Completion Date
October 2015 (Actual)
Study Completion Date
December 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Uppsala University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Previous trials have demonstrated that the use of physiological assessment of stenosis severity using fractional flow reserve (FFR) is superior to angiographic assessment in percutaneous coronary intervention (PCI) and improves clinical outcome. Despite the clinical utility, FFR is used only in 10-15% of patients today. The main reasons for the low adoption rate of FFR are the prolonged procedural time, Adenosine related discomfort and cost associated with Adenosine. Instantaneous Wave-Free ratio (iFR®) is a novel method to assess coronary lesions for functional significance. The main benefits of the method compared to FFR are that the measurement is instantaneous and does not require Adenosine infusion. Thus, the patient does not experience any discomfort from the measurement and procedural time could be shortened compared to when using FFR. This could potentially increase the adoption rate of physiologic assessment of coronary lesions. The aim of this trial is to compare the clinical outcome of patients assessed by iFR® with patients assessed by FFR. Furthermore, the trial will be conducted as a registry based randomized clinical trial (RRCT) which is a novel strategy to conduct clinical trials. The randomization will occur online in the Swedish angiography and angioplasty registry (SWEDEHEART) using a web based platform.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Angina Pectoris, Acute Myocardial Infarction
Keywords
Instantaneous wave Free Ratio, Fractional Flow Reserve

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
2037 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Instantaneous wave-free ratio (iFR)
Arm Type
Experimental
Arm Title
Fractional Flow Reserve (FFR)
Arm Type
Active Comparator
Intervention Type
Device
Intervention Name(s)
iFR
Intervention Description
Treatment guided by Instantaneous wave-free ratio (iFR®)
Intervention Type
Device
Intervention Name(s)
FFR
Intervention Description
Intervention guided by Fractional Flow Reserve
Primary Outcome Measure Information:
Title
All cause death, non-fatal Myocardial infarction (MI), Unplanned revascularization
Time Frame
12 months
Secondary Outcome Measure Information:
Title
All cause death
Time Frame
1-5 years
Title
Non-fatal MI
Time Frame
1-5 years
Title
Unplanned revascularization
Time Frame
1-5 years
Title
Target lesion revascularization
Time Frame
1-5 years
Title
Time to acute coronary occlusion, stent thrombosis and restenosis in treated lesions as reported in Swedish Coronary Angiography and Angioplasty Registry (SCAAR)
Time Frame
1-5 years
Title
Change in physician´s treatment strategy depending on iFR/FFR information
Description
Before randomization, the operators will have to record their angiographic assessment of the coronary lesions and the theoretical treatment strategy based on the angiographic information alone. After randomization and functional assessment of lesion severity, the operators will record how iFR/FFR changed the treatment strategy.
Time Frame
Day 1
Title
Assessment of patient discomfort during the procedure (none/mild/moderate/severe
Time Frame
Day 1
Title
Procedural time
Time Frame
Day 1

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
99 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with suspected stable angina pectoris or unstable angina pectoris/non-ST-segment elevation myocardial infarction (NSTEMI) who are scheduled to undergo coronary angiography, and who has an indication for physiology guided assessment of coronary lesions (usually 30-80% stenosis grade). In patients with suspected stable angina pectoris, any lesion may be assessed. In patients with unstable angina pectoris/NSTEMI, only the non-culprit lesion may be assessed. Exclusion Criteria: Inability to provide informed consent Age below 18 years Previous randomization in the iFR-SWEDEHEART trial Known terminal disease with a life expectancy of less than one year. In patients with multi-vessel disease and other indication than stable angina pectoris, difficulty in assessing which the culprit lesion is. Patient with unstable hemodynamics (Killip class III-IV) Inability to tolerate Adenosine Previous Coronary artery bypass graft (CABG) with patent grafts to the interrogated vessel. Heavily calcified or tortuous vessel where inability to cross the lesion with a pressure wire is expected.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Matthias Götberg, MD,PhD
Organizational Affiliation
Department of Cardiology, Skane University Hospital, Lund University, Lund, Sweden
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ole Fröbert, Prof
Organizational Affiliation
Department of Cardiology, Örebro University Hospital, Örebro, Sweden
Official's Role
Study Chair
Facility Information:
Facility Name
Skejby University Hospital
City
Aarhus
Country
Denmark
Facility Name
Reykjavik University Hospital
City
Reykjavik
Country
Iceland
Facility Name
Sahlgrenska University Hospital
City
Göteborg
Country
Sweden
Facility Name
Halmstad sjukhus
City
Halmstad
Country
Sweden
Facility Name
Helsingborg County Hospital
City
Helsingborg
Country
Sweden
Facility Name
Kalmar County Hospital
City
Kalmar
Country
Sweden
Facility Name
Karlstad County Hospital
City
Karlstad
Country
Sweden
Facility Name
Linköping University Hospital
City
Linköping
Country
Sweden
Facility Name
Skane University Hospital
City
Lund
Country
Sweden
Facility Name
S:t Göran County Hospital
City
Stockholm
Country
Sweden
Facility Name
Sundsvall County Hospital
City
Sundsvall
Country
Sweden
Facility Name
Uppsala University Hospital
City
Uppsala
Country
Sweden
Facility Name
Västerås County Hospital
City
Västerås
Country
Sweden
Facility Name
Örebro University Hospital
City
Örebro
Country
Sweden

12. IPD Sharing Statement

Citations:
PubMed Identifier
35272801
Citation
Gotberg M, Berntorp K, Rylance R, Christiansen EH, Yndigegn T, Gudmundsdottir IJ, Koul S, Sandhall L, Danielewicz M, Jakobsen L, Olsson SE, Olsson H, Omerovic E, Calais F, Lindroos P, Maeng M, Venetsanos D, James SK, Karegren A, Carlsson J, Jensen J, Karlsson AC, Erlinge D, Frobert O. 5-Year Outcomes of PCI Guided by Measurement of Instantaneous Wave-Free Ratio Versus Fractional Flow Reserve. J Am Coll Cardiol. 2022 Mar 15;79(10):965-974. doi: 10.1016/j.jacc.2021.12.030.
Results Reference
derived
PubMed Identifier
28317438
Citation
Gotberg M, Christiansen EH, Gudmundsdottir IJ, Sandhall L, Danielewicz M, Jakobsen L, Olsson SE, Ohagen P, Olsson H, Omerovic E, Calais F, Lindroos P, Maeng M, Todt T, Venetsanos D, James SK, Karegren A, Nilsson M, Carlsson J, Hauer D, Jensen J, Karlsson AC, Panayi G, Erlinge D, Frobert O; iFR-SWEDEHEART Investigators. Instantaneous Wave-free Ratio versus Fractional Flow Reserve to Guide PCI. N Engl J Med. 2017 May 11;376(19):1813-1823. doi: 10.1056/NEJMoa1616540. Epub 2017 Mar 18.
Results Reference
derived
PubMed Identifier
26542503
Citation
Gotberg M, Christiansen EH, Gudmundsdottir I, Sandhall L, Omerovic E, James SK, Erlinge D, Frobert O. Instantaneous Wave-Free Ratio versus Fractional Flow Reserve guided intervention (iFR-SWEDEHEART): Rationale and design of a multicenter, prospective, registry-based randomized clinical trial. Am Heart J. 2015 Nov;170(5):945-50. doi: 10.1016/j.ahj.2015.07.031. Epub 2015 Aug 15.
Results Reference
derived

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Evaluation of iFR vs FFR in Stable Angina or Acute Coronary Syndrome

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