CClinicalTrials.gg
RecruitingNCT05329285STICHUpdated Jun 24, 2024

CABG or PCI in Patients With Ischemic Cardiomyopathy

An interventional study of Percutaneous Coronary Intervention (PCI) in Coronary Artery Disease, sponsored by Vastra Gotaland Region. Recruiting at 1 site in Sweden. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-06-24.

Sponsored by Vastra Gotaland Region · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Started Sep 2022; still recruiting 4 years later.
Phase
Not applicable
Study type
Interventional
Enrollment
470
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The STICH-SWEDEHEART trial will compare PCI vs CABG for revascularization of patients with HF and LV systolic dysfunction (LV ejection fraction (LVEF) \<40%) and multi-vessel coronary artery disease.

Read the detailed description

Short background/ Rationale/Aim:

CABG has been shown to prolong survival in patients with reduced left ventricular (LV) function and multi-vessel coronary artery disease and "CABG is recommended as the first revascularization strategy choice in patients with multi-vessel disease and acceptable surgical risk". However, a major concern with CABG is the early risk of complications, including death and stroke. Although PCI has lower rates of peri-procedural complications than CABG in patients without heart failure (HF), this has not been confirmed in patients with HF. The lack of contemporary data comparing CABG and PCI in HF leaves clinicians with no guidance as to which option to choose, and a robust trial is therefore necessary. The STICH-SWEDEHEART trial will compare PCI vs CABG for revascularization of patients with HF and LV systolic dysfunction (LV ejection fraction (LVEF) \< 40%) and multi-vessel coronary artery disease.

Study objective:

To test whether PCI is non-inferior to CABG for revascularization of patients with ischemic heart failure.

Study design:

Multicentre, open-label, randomized controlled trial

Study population:

Patients with ischemic cardiomyopathy and reduced ejection fraction.

Number of subjects:

470 subjects

Investigational treatment:

PCI

Treatment in control group:

CABG

Study endpoints:

Primary endpoint (variable):

The occurrence of the composite of death, stroke, non-procedural myocardial infarction or heart failure hospitalization at 3 years.

Key secondary endpoint The hierarchical occurrence (in descending order of importance) at 3-year follow-up of time to death, time to stroke, time to non-procedural myocardial infarction, number of heart failure hospitalizations and 1-year Kansas City Cardiomyopathy Questionnaire (KCCQ) score; evaluated using the win ratio approach.

Secondary safety endpoints

In-hospital occurrence of the following:

  1. Death
  2. Stroke
  3. Non-procedural myocardial infarction
  4. The occurrence of in-hospital BARC ≥3 bleeding

    Time to the occurrence of the following:

  5. Mediastinitis
  6. Pericardial tamponade Other secondary endpoints
  1. Time to the occurrence of the following: A. Death, stroke or non-procedural myocardial infarction B. Death or heart failure hospitalization C. Heart failure hospitalization D. Coronary revascularization E. Death or myocardial infarction F. Death or stroke 2. Total number of days in-hospital during index hospitalization 3. Total number of days in intensive care unit during index hospitalization 4. Quality of life at 30 days and 365 days.
02

Conditions studied

  • Coronary Artery Disease

Keywords

  • PCI
  • CABG
03

In context

Coronary Artery Disease

5,598 studies on the registry are indexed under Coronary Artery Disease; 957 are open to participants now.

This study's planned enrollment of 470 is above the median of 124 across 3,436 interventional studies indexed under Coronary Artery Disease.

Browse Coronary Artery Disease studies →

Lead sponsor

Vastra Gotaland Region is the lead sponsor of 267 studies on the registry; 107 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. Age ≥18 years.
  2. Symptomatic HF defined as NYHA HF class II-IV within 1 month of enrolment
  3. LVEF ≤ 40% quantified by either echocardiography or gated SPECT ventriculography, or magnetic resonance (MR) or any other recognized assessment of LVEF
  4. Meaningful amount of myocardium at risk because of CAD (BCIS myocardial jeopardy score ≥ 6 on a recent (> 6 months) coronary angiogram);
  5. Heart team believes that a meaningful revascularization can be achieved by both PCI or CABG, with complete revascularization defined as residual ischemia in \<10% of the left ventricle
  6. Heart team agrees that guideline directed medical therapy (GDMT) has been initiated for ≥1 month in prevalent and newly diagnosed cases. In patients hospitalized with newly diagnosed iLVSD (with or without acute coronary syndrome (ACS)) requiring revascularization before discharge, GDMT needs to be initiated, when possible, in-hospital before randomization, with the expectation that it will be titrated to maximally tolerated doses after revascularization
  7. Written informed consent obtained

Exclusion criteria

Exclusion Criteria:

  1. Previous randomization in the study
  2. Decompensated heart failure requiring inotropic /adrenergic support, invasive or non-invasive ventilation or intra-aortic balloon pump/ventricular assist device therapy less than 48 hours prior to randomization
  3. Recent (\<1 month) type 1 myocardial infarction
  4. Recent PCI (\<3 months)
  5. Valvular heart disease or any other cardiac conditions (e.g. LV aneurysm) requiring surgical repair/replacement
  6. Prohibitive bleeding risk or clinical scenario mandating avoidance of long-term dual antiplatelet therapy
  7. Expected survival less than 3 years due to non-cardiac illness
  8. Circumstances likely to lead to poor treatment compliance
  9. Individuals for whom record in public health databases is not accessible (non-eligibility to public health system, parallel healthcare systems
  10. Pregnancy or woman of childbearing potential who is not sterilized or using a medically accepted form of contraception
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
470 participants (estimated)

Study arms

  • Experimental
    Percutaneous Coronary Intervention (PCI)

    Patients will be revascularized by PCI

    Procedure: Percutaneous Coronary Intervention (PCI)

  • No intervention
    Coronary artery bypass grafting (CABG)

    Patients will be revascularized by CABG

Interventions

  • ProcedurePercutaneous Coronary Intervention (PCI)

    Alternative treatment

06

What researchers measure

Primary outcomes

  1. Major adverse cardiac event

    The occurrence of the composite of death, stroke, non-procedural myocardial infarction or heart failure hospitalization

    Time frame: 3 years

Secondary outcomes

  1. The occurrence of death

    Time to death

    Time frame: 3 years

  2. The occurrence of stroke

    Time to stroke

    Time frame: 3 year

  3. The occurrence of non-procedural myocardial infarction,

    Time to non-procedural myocardial infarction,

    Time frame: 3 year

  4. The occurrence of heart failure hospitalizations

    Number of heart failure hospitalizations

    Time frame: 3 year

  5. Kansas City Cardiomyopathy Questionnaire (KCCQ) score

    Kansas City Cardiomyopathy Questionnaire score; evaluated using the win ratio approach. High score mean a better outcome

    Time frame: 1 year

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 24, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05329285
Lead sponsor
Vastra Gotaland Region
Collaborators
Region Örebro County, Karolinska University Hospital, University Hospital, Umeå
Responsible party
Sponsor
First posted
Apr 15, 2022
Start date
Sep 14, 2022
Primary completion
Dec 31, 2028 (estimated)
Completion
Dec 31, 2052 (estimated)
Last update
Jun 24, 2024

Study contacts

Björn Redfors, MD, PhD
Contact
Bjoern.Redfors@wlab.gu.se
+46313427543
Elmir Omerovic, MD, PhD
Contact
elmir@wlab.gu.se
+46 31 3421000

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

Contact study team

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion