STem cElls Mobilization in Acute Myocardial Infarction Outcome Trial (STEM-AMI)

This study is currently recruiting participants. (see Contacts and Locations)
Verified March 2014 by Heart Care Foundation
Sponsor:
Collaborators:
A. Manzoni Hospital
Centro Cardiologico Monzino
Information provided by (Responsible Party):
Heart Care Foundation
ClinicalTrials.gov Identifier:
NCT01969890
First received: October 22, 2013
Last updated: March 17, 2014
Last verified: March 2014

October 22, 2013
March 17, 2014
October 2013
October 2016   (final data collection date for primary outcome measure)
The composite endpoint of: - All cause death or, - recurrence of myocardial infarction (MI) or, - hospitalization due to heart failure. [ Time Frame: two years ] [ Designated as safety issue: Yes ]
Same as current
Complete list of historical versions of study NCT01969890 on ClinicalTrials.gov Archive Site
- All cause death and cardiovascular events [ Time Frame: two years ] [ Designated as safety issue: Yes ]

The following Cardiovascular events will be assessed:

  • recurrence of MI,
  • hospitalization due to heart failure,
  • cardiovascular death,
  • coronary revascularization,
  • fatal and non fatal stroke,
  • hospitalization due to any cause,
  • cardiovascular hospitalization,
  • resuscitation and/or appropriate automated implanted cardioverter defibrillator(AICD) therapy.
Same as current
Safety endpoints - Incidence and severity of bleeding complications, - incidence of malignancy, - incidence and intensity of serious adverse events (SAEs) and adverse drug reactions (ADRs) [ Time Frame: two years ] [ Designated as safety issue: Yes ]
Same as current
 
STem cElls Mobilization in Acute Myocardial Infarction Outcome Trial
Phase III Study on STem cElls Mobilization in Acute Myocardial Infarction

The purpose of this study is to demonstrate that granulocyte colony-stimulating factor (G-CSF) therapy in addition to state-of-the-art treatment (pharmacological and non pharmacological) is safe and significantly improves clinical outcome in patients with reduced left ventricular ejection fraction (LVEF) (≤45%) after successful reperfusion for large anterior acute myocardial infarction.

Not Provided
Interventional
Phase 3
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
  • Anterior Acute Myocardial Infarction
  • Left Ventricular Systolic Dysfunction
Drug: G-CSF administration
Zarzio - 5 microg/kg bis in die for 6 days
Other Name: Zarzio
  • Experimental: G-CSF
    Zarzio - 5 microg/kg bis in die for 6 days
    Intervention: Drug: G-CSF administration
  • No Intervention: standard therapy
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
1530
October 2018
October 2016   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Patients affected by acute anterior ST elevation myocardial infarction (STEMI) undergoing primary percutaneous coronary intervention (PCI) or PCI-rescue with persistent occlusion of coronary artery,
  • Time symptom-to-balloon (≥3 h and ≤12h or ≤24 h if symptoms persist),
  • Thrombolysis in Myocardial Infarction (TIMI) flow post PCI ≥2,
  • Evidence of left ventricular (LV) dysfunction (EF biplane ≤45%) ≤24 h after revascularization,
  • Men and women aged ≥18 years and ≤75 years,
  • Informed consent must be signed before proceeding with any study procedure.

Exclusion Criteria:

  • Previous anterior MI,
  • Recent MI (within 1 month),
  • Known previous LV dysfunction (EF <45%),
  • Patients with angiographic evidence of coronary anatomy not suitable for PCI, or needing coronary artery bypass grafting (CABG),
  • Valve disease requiring surgical correction,
  • History of previous cardiac surgery or PCI on LAD within 6 months,
  • Previous or current documented history of leukemia, myeloproliferative or myelodysplastic disorder,
  • Previous or current documented history of malignant disease,
  • Haemoglobin <10 mg/dl,
  • White blood cells (WBC) >25.000 mm3,
  • Platelet <50.000 mm3,
  • Sepsis,
  • Known HIV infection,
  • Immune system diseases,
  • Interstitial lung disease
  • Serious concomitant medical conditions (other than ischemic heart disease),
  • Pregnancy and breast feeding,
  • Documented alcohol and drug abuse,
  • Anticipated poor compliance.
  • Current participation in a clinical trial with other investigational products
  • Other cell therapy.
Both
18 Years to 75 Years
No
Contact: Aldo P. Maggioni, MD +39-055-5101361 centrostudi@anmco.it
Italy
 
NCT01969890
G112
Yes
Heart Care Foundation
Heart Care Foundation
  • A. Manzoni Hospital
  • Centro Cardiologico Monzino
Study Chair: Felice Achilli, MD Ospedale Alessandro Manzoni - Lecco
Study Chair: Giulio Pompilio, MD Centro Cardiologico Monzino - Milano
Heart Care Foundation
March 2014

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP