Postconditioning in ST-elevation Myocardial Infarction (POSTEMI)
Primary Purpose
Myocardial Infarction
Status
Completed
Phase
Not Applicable
Locations
Norway
Study Type
Interventional
Intervention
Postconditioning
Control intervention
Sponsored by
About this trial
This is an interventional treatment trial for Myocardial Infarction focused on measuring ST-elevation myocardial infarction
Eligibility Criteria
Inclusion Criteria:
- acute symptoms consistent with an acute myocardial infarction of less than 6 hours duration
- an occluded infarct related artery must be demonstrated (TIMI-flow 0-1)
Exclusion Criteria:
- Prior myocardial infarction
- Demonstration of collaterals to the infarcted area
- TIMI-flow >1 before intervention or TIMI-flow <2 after initial balloon inflation
- Demonstration of a distal occlusion
- Patients given thrombolytic treatment
- Patients in cardiogenic shock
- Any contraindication to MRI (magnetic resonance imaging)
- Unwillingness to participate
Sites / Locations
- Dept. of Cardiology, Oslo Univ. Hosp. Ulleval
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Other
Arm Label
Postconditioning
Control
Arm Description
Active arm:Postconditioning protocol before routine PCI/stenting of an occluded coronary artery
Control arm: Routine PCI/stenting of an occluded coronary artery without postconditioning
Outcomes
Primary Outcome Measures
Infarct size, assessed by MRI
Secondary Outcome Measures
Myocardial blushing grade
ST-resolution in ECG
Troponin-T and CK-MB
Echocardiographic evaluation of left ventricular function including speckle-tracking measurement.
Assesment of LV function. Comparison with CMR in the whole study population and between treatment groups.
Incidence of treated arrhythmias and heart failure during initial hospitalization Incidence of death, non-fatal myocardial infarction, unstable angina, heart failure, and cerebrovascular disease
Myocardial salvage
Myocardial salvage defined as (area at risk-final infarct size)/area at risk. Area at risk measured by CMR at baseline and final infarct size by CMR at 4 months.
Full Information
NCT ID
NCT00922675
First Posted
June 16, 2009
Last Updated
September 26, 2016
Sponsor
Oslo University Hospital
1. Study Identification
Unique Protocol Identification Number
NCT00922675
Brief Title
Postconditioning in ST-elevation Myocardial Infarction
Acronym
POSTEMI
Official Title
Postconditioning in ST-elevation Myocardial Infarction Treated With Primary PCI
Study Type
Interventional
2. Study Status
Record Verification Date
September 2016
Overall Recruitment Status
Completed
Study Start Date
June 2009 (undefined)
Primary Completion Date
August 2012 (Actual)
Study Completion Date
August 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Oslo University Hospital
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Study objectives: To assess the effects of postconditioning on infarct size in patients with ST-elevation infarction referred to PCI.
Study design: Prospective, randomized, open-label study with blinded endpoint evaluation. Included patients will be randomly allocated to postconditioning or control. Patients with symptoms of acute myocardial infarction of less than 6 hours duration fulfilling ECG criteria for primary PCI are eligible. PCI follow established routines. In postconditioning patients, additional, short (1 min), intermittent balloon occlusions will be applied after initial opening of infarct related artery. After this intervention, PCI proceeds routinely with stent implantation. In the control group, stent implantation after initial opening proceeds as usual. Primary endpoint is final infarct size, determined by MRI after 4 months. 260 patients will be included. Follow-up is 1 year. Inclusion period: 18 - 24 months.
Clinical implications: Reperfusion therapy, administered as early as possible after start of symptoms, has improved the prognosis in acute ST-elevation myocardial infarction. Still, however, many patients suffer large infarctions, subsequently with an increased risk of heart failure, arrhythmias, and death. In pilot studies, mechanical postconditioning has been shown to reduce infarct size and thus potentially improve prognosis. However, the effect of postconditioning must be confirmed in larger clinical trials before implemented in routine treatment.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Myocardial Infarction
Keywords
ST-elevation myocardial infarction
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
272 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Postconditioning
Arm Type
Experimental
Arm Description
Active arm:Postconditioning protocol before routine PCI/stenting of an occluded coronary artery
Arm Title
Control
Arm Type
Other
Arm Description
Control arm: Routine PCI/stenting of an occluded coronary artery without postconditioning
Intervention Type
Procedure
Intervention Name(s)
Postconditioning
Intervention Description
After opening of IRA and establishment of TIMI-flow grade 2 or 3, the control group continues the procedure with stenting. In the postconditioning group 4 additional balloon inflations separated by 1 minute reperfusion are given, starting after 1 minute of reperfusion.
Intervention Type
Procedure
Intervention Name(s)
Control intervention
Intervention Description
After opening of IRA and establishment of TIMI-flow grade 2 or 3, the control group continues the procedure with stenting.
Primary Outcome Measure Information:
Title
Infarct size, assessed by MRI
Time Frame
4 months
Secondary Outcome Measure Information:
Title
Myocardial blushing grade
Time Frame
assessed at the end of PCI procedure
Title
ST-resolution in ECG
Time Frame
Assessed after 1 hour
Title
Troponin-T and CK-MB
Time Frame
peak release values
Title
Echocardiographic evaluation of left ventricular function including speckle-tracking measurement.
Description
Assesment of LV function. Comparison with CMR in the whole study population and between treatment groups.
Time Frame
assessed at baseline, 4 months and1 year
Title
Incidence of treated arrhythmias and heart failure during initial hospitalization Incidence of death, non-fatal myocardial infarction, unstable angina, heart failure, and cerebrovascular disease
Time Frame
1-year follow up.
Title
Myocardial salvage
Description
Myocardial salvage defined as (area at risk-final infarct size)/area at risk. Area at risk measured by CMR at baseline and final infarct size by CMR at 4 months.
Time Frame
Baseline to 4 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
acute symptoms consistent with an acute myocardial infarction of less than 6 hours duration
an occluded infarct related artery must be demonstrated (TIMI-flow 0-1)
Exclusion Criteria:
Prior myocardial infarction
Demonstration of collaterals to the infarcted area
TIMI-flow >1 before intervention or TIMI-flow <2 after initial balloon inflation
Demonstration of a distal occlusion
Patients given thrombolytic treatment
Patients in cardiogenic shock
Any contraindication to MRI (magnetic resonance imaging)
Unwillingness to participate
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jan Eritsland, MD, PhD
Organizational Affiliation
Oslo Univ.Hosp. Ulleval
Official's Role
Study Chair
Facility Information:
Facility Name
Dept. of Cardiology, Oslo Univ. Hosp. Ulleval
City
Oslo
ZIP/Postal Code
N-0407
Country
Norway
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
34933964
Citation
Tollefsen IM, Shetelig C, Seljeflot I, Eritsland J, Hoffmann P, Andersen GO. High levels of interleukin-6 are associated with final infarct size and adverse clinical events in patients with STEMI. Open Heart. 2021 Dec;8(2):e001869. doi: 10.1136/openhrt-2021-001869.
Results Reference
derived
PubMed Identifier
24760962
Citation
Limalanathan S, Andersen GO, Klow NE, Abdelnoor M, Hoffmann P, Eritsland J. Effect of ischemic postconditioning on infarct size in patients with ST-elevation myocardial infarction treated by primary PCI results of the POSTEMI (POstconditioning in ST-Elevation Myocardial Infarction) randomized trial. J Am Heart Assoc. 2014 Apr 23;3(2):e000679. doi: 10.1161/JAHA.113.000679.
Results Reference
derived
Learn more about this trial
Postconditioning in ST-elevation Myocardial Infarction
We'll reach out to this number within 24 hrs