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. 2019 Feb 20;21(8):1032–1041. doi: 10.1002/ejhf.1412

Table 1.

Inclusion and exclusion criteria of the SCIENCE trial

Inclusion criteria Exclusion criteria
  • 30–80 years of age

  • Signed informed consent

  • Chronic stable ischaemic heart disease

  • Symptomatic HF (NYHA class II–III)

  • LVEF ≤ 45% on echocardiography, CT or MRI scan

  • Plasma NT‐proBNP > 300 pg/mL (> 35 pmol/L)

  • Maximal tolerable HF medication unchanged 2 months prior to inclusion

  • No option for PCI or CABG

  • Patients who have had PCI or CABG within 6 months of inclusion must have a new coronary angiography to rule out early restenosis

  • Patients cannot be included until 3 months after implantation of a CRT‐D and until 1 month after an ICD unit

  • HF NYHA class I or IV

  • Acute coronary syndrome within 6 weeks of inclusion

  • Other revascularization treatment within 4 months of treatment

  • Moderate to severe aortic stenosis (valve area < 1.3 cm2) or valvular disease with option for surgery or interventional therapy

  • Aortic valve replacement with an artificial heart valve. However, a trans‐septal treatment approach can be considered in these patients

  • If the patient is expected to be candidate for MitraClip therapy

  • Diminished functional capacity for other reasons such as COPD with FEV1 < 1 L/min, moderate to severe claudication or morbid obesity

  • Clinical significant anaemia (Hb < 6 mmol/L), leukopenia (leucocytes < 2 × 109/L), leukocytosis (leucocytes > 14 × 109/L) or thrombocytopenia (thrombocytes < 50 × 109/L)

  • Reduced kidney function (eGFR < 30 mL/min)

  • Left ventricular thrombus

  • Anticoagulation treatment that cannot be paused during cell injections

  • Patients with reduced immune response or known anti‐HLA antibodies

  • History with malignant disease within 5 years of inclusion or suspected malignancy – except treated skin cancer other than melanoma

  • Pregnant women

  • Other experimental treatment within 4 weeks of baseline tests

  • Life expectancy < 1 year

  • Participation in another intervention trial

  • Known hypersensitivity to DMSO, penicillin and streptomycin

CABG, coronary artery bypass graft; COPD, chronic obstructive pulmonary disease; CRT‐D, cardiac resynchronization therapy with defibrillation; CT, computed tomography; DMSO, dimethyl sulfoxide; eGFR, estimated glomerular filtration rate; FEV1, forced expiratory volume in 1 s; Hb, haemoglobin; HF, heart failure; HLA, human leucocyte antigen; ICD, implantable cardioverter defibrillator; LVEF, left ventricular ejection fraction; MRI, magnetic resonance imaging; NT‐proBNP, N‐terminal pro‐B‐type natriuretic peptide; NYHA, New York Heart Association; PCI, percutaneous coronary intervention.