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SWiss Multicenter Intracoronary Stem Cells Study in Acute Myocardial Infarction (SWISS-AMI)

Primary Purpose

Acute Myocardial Infarction

Status
Completed
Phase
Phase 2
Locations
Switzerland
Study Type
Interventional
Intervention
intracoronary bone marrow cells infusion
Sponsored by
University of Zurich
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Myocardial Infarction focused on measuring acute myocardial infarction, MRI, bone marrow cells, stem cells, remodeling

Eligibility Criteria

18 Years - 90 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Visual LVEF at angiogram or echocardiography ≤45% Treatment by primary PCI within 24 hours of the onset of chest pain or initial treatment with thrombolysis within the 12 hours followed by PCI within the 24 hours of the onset of chest pain Significant regional LV wall motion dysfunction in the infarct related territory Age >18 years Exclusion Criteria: Abnormal regional wall motion outside the infarct region Known previous myocardial infarction in the same target vessel Known pre-existing left ventricular dysfunction (EF<45% prior to admission) Need for revascularization in the non infarct-related coronary within 4 months Pre-existing symptoms of heart failure or known cardiomyopathy Known active infection or chronic infection with HIV, HBV or HCV Chronic inflammatory disease Serious concomitant disease with a life expectancy of less than one year Follow up impossible (no fixed abode, etc) Contraindication for cardiac MRI (i.e. pace maker, neurostimulator, claustrophobia) Severe renal failure (creatinine >250 mmol/l) Relevant liver disease (GOT > 2x norm or spontaneous INR > 1,5) Anemia (Hb < 8.5 mg/dl), Thrombocytopenia (<100.000/µl) Pregnancy Participation at a clinical trial in the last 30 days

Sites / Locations

  • Cardiology, University Hospital Berne
  • Kantonsspital
  • Cardiocentro Ticino
  • Cardiology, university Hospital Zurich

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

No Intervention

Experimental

Experimental

Arm Label

Control

Early

Late

Arm Description

Outcomes

Primary Outcome Measures

Change in global left ventricular ejection fraction (LVEF) at 4 months relative to baseline measured by quantitative MRI

Secondary Outcome Measures

Change in LVEF at MRI at 12 months
Change in regional left ventricular wall motion and thickness at 4 and 12 months
Change in infarct size at 4 and 12 months as assessed by "delayed enhancement" technique by MRI
Analysis of the myocardial infarct size and transmurality transmurality, time to PCI and coronary flow characteristics after PCI as predictor of LV remodeling and change after cell therapy
Change in myocardial perfusion at 4 and 12 months
Change in serum level of amino-terminal pro-brain natriuretic peptide (NT pro-BNP)
Major adverse cardiac events (MACE: death, myocardial infarction, TVR (ACBP or PCI, stroke, hospitalization for cardiac reasons) at 12 months

Full Information

First Posted
July 20, 2006
Last Updated
November 8, 2012
Sponsor
University of Zurich
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1. Study Identification

Unique Protocol Identification Number
NCT00355186
Brief Title
SWiss Multicenter Intracoronary Stem Cells Study in Acute Myocardial Infarction (SWISS-AMI)
Official Title
SWiss Multicenter Intracoronary Stem Cells Study in Acute Myocardial Infarction (SWISS-AMI)
Study Type
Interventional

2. Study Status

Record Verification Date
November 2012
Overall Recruitment Status
Completed
Study Start Date
August 2006 (undefined)
Primary Completion Date
October 2012 (Actual)
Study Completion Date
November 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Zurich

4. Oversight

5. Study Description

Brief Summary
Title: SWiss multicenter Intracoronary Stem cells Study in Acute Myocardial Infarction (SWISS-AMI). Study population: Patients with acute myocardial infarction, treated with primary PCI. Objective: To determine whether intracoronary infusion of BMCs improves recovery of left ventricular function after acute myocardial infarction treated by PCI Design: Multi-center, randomized, controlled clinical trial with central core lab analysis for MRI. Therapy: Intracoronary infusion of BMCs in the infarct related artery at 5-7 days or 3-4 weeks after successful primary PCI Primary Endpoint: Change in global left ventricular ejection fraction (LVEF) at 4 months relative to baseline measured by quantitative MRI. Secondary Endpoints: Change in LVEF at MRI at 12 months Change in regional left ventricular wall motion and thickness at 4 and 12 months. Change in infarct size at 4 and 12 months as assessed by "delayed enhancement" technique by MRI Analysis of the myocardial infarct size and transmurality, time to PCI and coronary flow characteristics after PCI as predictor of LV remodeling and change after cell therapy Change in myocardial perfusion at 4 and 12 months Change in serum level of amino-terminal pro-brain natriuretic peptide (NT pro-BNP) Major adverse cardiac events (MACE: death, myocardial infarction, TVR (ACBP or PCI, stroke, hospitalization for cardiac reasons) at 12 months Interventions: Aspiration of 50 ml bone marrow (<24 hours) prior to administration Intracoronary balloon-based infusion of 10 ml BMCs Cardiac MRI at baseline (resp. at hospital discharge), at 4 and 12 months Therapy groups: Bone marrow-derived stem cells infusion in the successfully revascularized infarct related vessel at day 5-7 or day 21-28. Control group: Management according to the "state of the art" medical therapy after successful primary PCI. Safety: A study independent "safety committee" will analyze the clinical results after the first 60 patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Myocardial Infarction
Keywords
acute myocardial infarction, MRI, bone marrow cells, stem cells, remodeling

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
200 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control
Arm Type
No Intervention
Arm Title
Early
Arm Type
Experimental
Arm Title
Late
Arm Type
Experimental
Intervention Type
Procedure
Intervention Name(s)
intracoronary bone marrow cells infusion
Intervention Description
intracoronary bone marrow cell infusion via a OTW balloon; "Stop-flow-technique" as previously described
Primary Outcome Measure Information:
Title
Change in global left ventricular ejection fraction (LVEF) at 4 months relative to baseline measured by quantitative MRI
Time Frame
4 months
Secondary Outcome Measure Information:
Title
Change in LVEF at MRI at 12 months
Time Frame
12 months
Title
Change in regional left ventricular wall motion and thickness at 4 and 12 months
Time Frame
4 and 12 months
Title
Change in infarct size at 4 and 12 months as assessed by "delayed enhancement" technique by MRI
Time Frame
4 and 12 months
Title
Analysis of the myocardial infarct size and transmurality transmurality, time to PCI and coronary flow characteristics after PCI as predictor of LV remodeling and change after cell therapy
Time Frame
baseline 4 and 12 months
Title
Change in myocardial perfusion at 4 and 12 months
Time Frame
4 and 12 months
Title
Change in serum level of amino-terminal pro-brain natriuretic peptide (NT pro-BNP)
Time Frame
4 and 12 months
Title
Major adverse cardiac events (MACE: death, myocardial infarction, TVR (ACBP or PCI, stroke, hospitalization for cardiac reasons) at 12 months
Time Frame
4 and 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Visual LVEF at angiogram or echocardiography ≤45% Treatment by primary PCI within 24 hours of the onset of chest pain or initial treatment with thrombolysis within the 12 hours followed by PCI within the 24 hours of the onset of chest pain Significant regional LV wall motion dysfunction in the infarct related territory Age >18 years Exclusion Criteria: Abnormal regional wall motion outside the infarct region Known previous myocardial infarction in the same target vessel Known pre-existing left ventricular dysfunction (EF<45% prior to admission) Need for revascularization in the non infarct-related coronary within 4 months Pre-existing symptoms of heart failure or known cardiomyopathy Known active infection or chronic infection with HIV, HBV or HCV Chronic inflammatory disease Serious concomitant disease with a life expectancy of less than one year Follow up impossible (no fixed abode, etc) Contraindication for cardiac MRI (i.e. pace maker, neurostimulator, claustrophobia) Severe renal failure (creatinine >250 mmol/l) Relevant liver disease (GOT > 2x norm or spontaneous INR > 1,5) Anemia (Hb < 8.5 mg/dl), Thrombocytopenia (<100.000/µl) Pregnancy Participation at a clinical trial in the last 30 days
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Roberto Corti, MD
Organizational Affiliation
Cardiology, University Hospital Zurich, Switzerland
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Thomas F Luescher, MD
Organizational Affiliation
Cardiology, University Hospital Zurich
Official's Role
Study Chair
Facility Information:
Facility Name
Cardiology, University Hospital Berne
City
Bern
Country
Switzerland
Facility Name
Kantonsspital
City
Lucerne
Country
Switzerland
Facility Name
Cardiocentro Ticino
City
Lugano
ZIP/Postal Code
6900
Country
Switzerland
Facility Name
Cardiology, university Hospital Zurich
City
Zurich
ZIP/Postal Code
8091
Country
Switzerland

12. IPD Sharing Statement

Citations:
PubMed Identifier
31982162
Citation
Gastl M, Surder D, Corti R, Faruque Osmany DMM, Gotschy A, von Spizcak J, Sokolska J, Metzen D, Alkadhi H, Ruschitzka F, Kozerke S, Manka R. Effect of intracoronary bone marrow-derived mononuclear cell injection early and late after myocardial infarction on CMR-derived myocardial strain. Int J Cardiol. 2020 Jul 1;310:108-115. doi: 10.1016/j.ijcard.2020.01.025. Epub 2020 Jan 15.
Results Reference
derived
PubMed Identifier
27267068
Citation
Surder D, Manka R, Moccetti T, Lo Cicero V, Emmert MY, Klersy C, Soncin S, Turchetto L, Radrizzani M, Zuber M, Windecker S, Moschovitis A, Buhler I, Kozerke S, Erne P, Luscher TF, Corti R. Effect of Bone Marrow-Derived Mononuclear Cell Treatment, Early or Late After Acute Myocardial Infarction: Twelve Months CMR and Long-Term Clinical Results. Circ Res. 2016 Jul 22;119(3):481-90. doi: 10.1161/CIRCRESAHA.116.308639. Epub 2016 Jun 6.
Results Reference
derived
PubMed Identifier
26098589
Citation
Surder D, Gisler V, Corti R, Moccetti T, Klersy C, Zuber M, Windecker S, Moschovitis A, Kozerke S, Luscher TF, Erne P, Manka R. Thrombus formation in the left ventricle after large myocardial infarction - assessment with cardiac magnetic resonance imaging. Swiss Med Wkly. 2015 Jun 22;145:w14122. doi: 10.4414/smw.2015.14122. eCollection 2015.
Results Reference
derived
PubMed Identifier
23596006
Citation
Surder D, Manka R, Lo Cicero V, Moccetti T, Rufibach K, Soncin S, Turchetto L, Radrizzani M, Astori G, Schwitter J, Erne P, Zuber M, Auf der Maur C, Jamshidi P, Gaemperli O, Windecker S, Moschovitis A, Wahl A, Buhler I, Wyss C, Kozerke S, Landmesser U, Luscher TF, Corti R. Intracoronary injection of bone marrow-derived mononuclear cells early or late after acute myocardial infarction: effects on global left ventricular function. Circulation. 2013 May 14;127(19):1968-79. doi: 10.1161/CIRCULATIONAHA.112.001035. Epub 2013 Apr 17.
Results Reference
derived
PubMed Identifier
20598973
Citation
Surder D, Schwitter J, Moccetti T, Astori G, Rufibach K, Plein S, Lo Cicero V, Soncin S, Windecker S, Moschovitis A, Wahl A, Erne P, Jamshidi P, Auf der Maur C, Manka R, Soldati G, Buhler I, Wyss C, Landmesser U, Luscher TF, Corti R. Cell-based therapy for myocardial repair in patients with acute myocardial infarction: rationale and study design of the SWiss multicenter Intracoronary Stem cells Study in Acute Myocardial Infarction (SWISS-AMI). Am Heart J. 2010 Jul;160(1):58-64. doi: 10.1016/j.ahj.2010.03.039.
Results Reference
derived

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SWiss Multicenter Intracoronary Stem Cells Study in Acute Myocardial Infarction (SWISS-AMI)

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