Safety of Early Discharge Following Low Risk Myocardial Infarction (EDAMI)
Primary Purpose
Myocardial Infarction
Status
Unknown status
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
early discharge (<72 h)
Conventional discharge
Sponsored by

About this trial
This is an interventional treatment trial for Myocardial Infarction focused on measuring myocardial infarction, primary percutaneous intervention, prognosis, early discharge
Eligibility Criteria
Inclusion Criteria:
- low risk (Zwolle risk score ≤3) STEMI treated with PPCI within 24 hours from symptoms onset
- Informed consent
Exclusion Criteria:
- arrhythmias (ventricular tachycardia or fibrillation, asystole, pulseless electrical activity, advanced atrio-ventricular block)
- mechanical complications (cardiac tamponade, free-wall or septal rupture, acute mitral regurgitation, pericarditis)
- severe or moderate bleeding (according to the GUSTO criteria)
- complications related to vascular access of the procedure
- acute kidney failure
- infection
- heart failure
Sites / Locations
- Hospital de la Santa Creu i Sant PauRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Early discharge (< 72 h)
Conventional discharge
Arm Description
Patients randomized the early discharge group will be discharged from the hospital in < 72 hours
Patients randomized to the conventional discharge group will be discharged according to the local hospital protocol and/or treating physician criterion
Outcomes
Primary Outcome Measures
All cause mortality, new acute myocardial infarction, new unstable angina, heart failure, ventricular arrhythmias, stroke and severe bleeding.
Composite primary end-point
Secondary Outcome Measures
All cause mortality
Myocardial infarction
Unstable angina
Heart failure
Ventricular arrhythmias
Stroke
Severe bleeding
According to the Global Use of Strategies to Open Occluded Coronary Arteries (GUSTO) classification
Full Information
NCT ID
NCT01868256
First Posted
November 23, 2012
Last Updated
May 30, 2013
Sponsor
Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
1. Study Identification
Unique Protocol Identification Number
NCT01868256
Brief Title
Safety of Early Discharge Following Low Risk Myocardial Infarction
Acronym
EDAMI
Official Title
Safety of a Early Discharge Strategy in Patients With Low-risk ST-segment Elevation Myocardial Infarction Treated With Primary Coronary Intervention: a Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
May 2013
Overall Recruitment Status
Unknown status
Study Start Date
January 2012 (undefined)
Primary Completion Date
January 2014 (Anticipated)
Study Completion Date
February 2014 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Objectives: The primary objective of this study is to evaluate the safety of an early discharge strategy in patients with low risk ST-elevation myocardial infarction (STEMI), treated with primary percutaneous coronary intervention (PPCI), compared to a conventional strategy.
Methodology: Unicentric, randomized, controlled, non-inferiority and open label clinical trial. The investigators will compare an early discharge strategy (≤72 hours) with a conventional strategy (discharge according to treating physician's criterion). Inclusion criteria will be: low risk (Zwolle risk score ≤3) STEMI treated with PPCI within 24 hours from symptoms onset. Exclusion criteria will be: arrhythmias (ventricular tachycardia or fibrillation, asystole, pulseless electrical activity, advanced atrio-ventricular block), mechanical complications (cardiac tamponade, free-wall or septal rupture, acute mitral regurgitation, pericarditis), severe or moderate bleeding (according to the GUSTO criteria), complications related to vascular access of the procedure, acute kidney failure, infection, heart failure. Sample size will be 1558 subjects (n=779 per group). The investigators will study demographic, clinical, biochemical, echocardiographic and angiographic variables. The primary endpoint will be a composite of death, reinfarction, new angina, heart failure, ventricular arrhythmias, stroke and severe bleeding. The secondary endpoint will include each of the items of the primary endpoint and quality of life and functional capacity questionnaire SF-36. Finally, the investigators will analyze the degree of compliance with the European Society of Cardiology guidelines on STEMI and the rate of hospitalization-related complications. Follow up will be at 30 days.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Myocardial Infarction
Keywords
myocardial infarction, primary percutaneous intervention, prognosis, early discharge
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1558 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Early discharge (< 72 h)
Arm Type
Experimental
Arm Description
Patients randomized the early discharge group will be discharged from the hospital in < 72 hours
Arm Title
Conventional discharge
Arm Type
Active Comparator
Arm Description
Patients randomized to the conventional discharge group will be discharged according to the local hospital protocol and/or treating physician criterion
Intervention Type
Other
Intervention Name(s)
early discharge (<72 h)
Intervention Type
Other
Intervention Name(s)
Conventional discharge
Primary Outcome Measure Information:
Title
All cause mortality, new acute myocardial infarction, new unstable angina, heart failure, ventricular arrhythmias, stroke and severe bleeding.
Description
Composite primary end-point
Time Frame
1 month
Secondary Outcome Measure Information:
Title
All cause mortality
Time Frame
1 month
Title
Myocardial infarction
Time Frame
1 month
Title
Unstable angina
Time Frame
1 month
Title
Heart failure
Time Frame
1 month
Title
Ventricular arrhythmias
Time Frame
1 month
Title
Stroke
Time Frame
1 month
Title
Severe bleeding
Description
According to the Global Use of Strategies to Open Occluded Coronary Arteries (GUSTO) classification
Time Frame
1 month
Other Pre-specified Outcome Measures:
Title
Difference in quality of life and functional capacity questionnaire SF-36.
Time Frame
1 month
Title
Compliance of treatment
Time Frame
1 month
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:
low risk (Zwolle risk score ≤3) STEMI treated with PPCI within 24 hours from symptoms onset
Informed consent
Exclusion Criteria:
arrhythmias (ventricular tachycardia or fibrillation, asystole, pulseless electrical activity, advanced atrio-ventricular block)
mechanical complications (cardiac tamponade, free-wall or septal rupture, acute mitral regurgitation, pericarditis)
severe or moderate bleeding (according to the GUSTO criteria)
complications related to vascular access of the procedure
acute kidney failure
infection
heart failure
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alessandro Sionis, MD
Organizational Affiliation
Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital de la Santa Creu i Sant Pau
City
Barcelona
ZIP/Postal Code
08025
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Alessandro Sionis, MD
Phone
+ 34 935565945
Email
asionis@santpau.cat
First Name & Middle Initial & Last Name & Degree
Alessandro Sionis, MD
12. IPD Sharing Statement
Citations:
PubMed Identifier
10717009
Citation
Newby LK, Eisenstein EL, Califf RM, Thompson TD, Nelson CL, Peterson ED, Armstrong PW, Van de Werf F, White HD, Topol EJ, Mark DB. Cost effectiveness of early discharge after uncomplicated acute myocardial infarction. N Engl J Med. 2000 Mar 16;342(11):749-55. doi: 10.1056/NEJM200003163421101.
Results Reference
background
PubMed Identifier
15159293
Citation
De Luca G, Suryapranata H, van 't Hof AW, de Boer MJ, Hoorntje JC, Dambrink JH, Gosselink AT, Ottervanger JP, Zijlstra F. Prognostic assessment of patients with acute myocardial infarction treated with primary angioplasty: implications for early discharge. Circulation. 2004 Jun 8;109(22):2737-43. doi: 10.1161/01.CIR.0000131765.73959.87. Epub 2004 May 24.
Results Reference
background
PubMed Identifier
9561995
Citation
Grines CL, Marsalese DL, Brodie B, Griffin J, Donohue B, Costantini CR, Balestrini C, Stone G, Wharton T, Esente P, Spain M, Moses J, Nobuyoshi M, Ayres M, Jones D, Mason D, Sachs D, Grines LL, O'Neill W. Safety and cost-effectiveness of early discharge after primary angioplasty in low risk patients with acute myocardial infarction. PAMI-II Investigators. Primary Angioplasty in Myocardial Infarction. J Am Coll Cardiol. 1998 Apr;31(5):967-72. doi: 10.1016/s0735-1097(98)00031-x.
Results Reference
background
PubMed Identifier
20102876
Citation
Kotowycz MA, Cosman TL, Tartaglia C, Afzal R, Syal RP, Natarajan MK. Safety and feasibility of early hospital discharge in ST-segment elevation myocardial infarction--a prospective and randomized trial in low-risk primary percutaneous coronary intervention patients (the Safe-Depart Trial). Am Heart J. 2010 Jan;159(1):117.e1-6. doi: 10.1016/j.ahj.2009.10.024.
Results Reference
background
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Safety of Early Discharge Following Low Risk Myocardial Infarction
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